Cathepsin
From Proteopedia
(New page: Crystal structure wild-type human procathepsin B, 1pbh {{STRUCTURE_1pbh| PDB=1pbh | SIZE=300| SCENE= |right|CAPTION=human procathepsin B, 1pbh...) |
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{{STRUCTURE_1pbh| PDB=1pbh | SIZE=300| SCENE= |right|CAPTION=human procathepsin B, [[1pbh]] }} | {{STRUCTURE_1pbh| PDB=1pbh | SIZE=300| SCENE= |right|CAPTION=human procathepsin B, [[1pbh]] }} | ||
| - | [[Cathepsin]] (CTS) is a protease which becomes activated at low pH. It is found in lysosomes. Members of the CTS group are denoted as CTSA, CTSB etc and cleave proteins at different peptide bonds. The CTSs are expressed as an inactive precursor pro-CTS (PCTS) which become active when a long residue prosegment is cleaved off producing the mature CTS (MCTS). | + | [[Cathepsin]] (CTS) is a protease which becomes activated at low pH. It is found in lysosomes. Members of the CTS group are denoted as CTSA, CTSB etc and cleave proteins at different peptide bonds. The CTSs are expressed as an inactive precursor pro-CTS (PCTS) which become active when a long residue prosegment is cleaved off producing the mature CTS (MCTS). The images at the left and at the right correspond to one representative Cathepsin, ''i.e.'' the crystal structure of wild-type human procathepsin B ([[1pbh]]). |
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| + | == 3D Structures of Cathepsin == | ||
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| + | === Procathepsin-B === | ||
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| + | [[1pbh]], [[2pbh]], [[3pbh]] – hPCTSB - human | ||
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| + | === Cathepsin-B mature === | ||
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| + | [[3hhi]] – TbCTSB (mutant) residues 23-340+CA074 – Trypanosoma brucei | ||
| + | [[3k9m]] – hMCTSB+stefin A | ||
| + | [[2ipp]], [[1huc]] – hMCTSB | ||
| + | [[3cbj]], [[3cbk]] – hMCTSB (mutant)+chagasin | ||
| + | [[2dc6]], [[2dc7]], [[2dc8]], [[2dc9]], [[2dca]], [[2dcb]], [[2dcc]], [[2dcd]] – bMCTSB+inhibitor – bovine | ||
| + | [[1sp4]], [[1csb]] – bMCTSB+epoxysuccinyl inhibitor | ||
| + | [[1ito]], [[1qdq]] – bMCTSB +inhibitor | ||
| + | [[1gmy]] - bMCTSB +dipeptidyl nitrile | ||
| + | [[1the]] – rMCTSB (mutant)+butanone inhibitor – rat | ||
| + | [[1cpj]] - rMCTSB (mutant) | ||
| + | [[1cte]] - rMCTSB+pyrimidine inhibitor | ||
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| + | === Cathepsin-C mature === | ||
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| + | [[2djf]], [[2djg]] – hMCTSC +Gly-Phe-CHN2 | ||
| + | [[1jqp]] – rMCTSC | ||
| + | [[1k3b]] – hMCTSC | ||
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| + | === Cathepsin-D mature === | ||
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| + | [[1lyw]], [[1lya]] – hMCTSD | ||
| + | [[1lyb]] - hMCTSD+pepstatin | ||
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| + | === Cathepsin-E mature === | ||
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| + | [[1tzs]] – hMCTSE+activation peptide from CTSE | ||
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| + | === Cathepsin-F mature === | ||
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| + | [[1m6d]] – hMCTSF+piperidine inhibitor | ||
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| + | === Cathepsin-G mature === | ||
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| + | [[1kyn]] – hMCTSG +naphthalene inhibitor | ||
| + | [[1au8]], [[1cgh]] - hMCTSG +phosphonate inhibitor | ||
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| + | === Cathepsin-H mature === | ||
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| + | [[1nb]]3, [[1nb5]] – pMCTSH +stefin A – pig | ||
| + | [[8pch]] - pMCTSH | ||
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| + | === Cathepsin-K mature === | ||
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| + | [[3o1g]], [[3n3g]], [[2r6n]], [[1bgo]], [[3kwz]], [[3kx1]] – hMCTSK+ pyrimidine inhibitor | ||
| + | [[3mpe]], [[3mpf]] – hMCTSK (mutant) + pyrimidine inhibitor | ||
| + | [[3h7d]] - hMCTSK (mutant) + chondroitin-4-sulfate | ||
| + | [[3c9e]] - hMCTSK + chondroitin-4-sulfate | ||
| + | [[3kwb]] - hMCTSK (mutant)+dioxo-triazine | ||
| + | [[3kw9]] - hMCTSK +triazine | ||
| + | [[1yk8]] - hMCTSK + cyanamide inhibitor | ||
| + | [[1yt7]] - hMCTSK + ketoamide inhibitor | ||
| + | [[2aux]], [[2auz]] - hMCTSK + semicarbazone inhibitor | ||
| + | [[1ayu]], [[1ayv]], [[1ayw]] - hMCTSK + carbohydrazide inhibitor | ||
| + | [[2bdl]], [[1yk7]], [[1tu6]], [[1au3]], [[1au4]] - hMCTSK + pyrrolidine inhibitor | ||
| + | [[1snk]] - hMCTSK + norleucine inhibitor | ||
| + | [[1nl6]], [[1nlj]] - hMCTSK+ azepanone inhibitor | ||
| + | [[1q6k]] - hMCTSK+carbamate inhibitor | ||
| + | [[1au0]] - hMCTSK+ diacylaminoethyl ketone inhibitor | ||
| + | [[1au2]] - hMCTSK+ propanone inhibitor | ||
| + | [[1atk]] – hMCTSK+guanidine inhibitor | ||
| + | [[1vsn]] - hMCTSK+ inhibitor | ||
| + | [[2ato]] – hMCTSK+myocrisin | ||
| + | [[1u9v]], [[1u9x]], [[1mem]] – hMCTSK+piperazine inhibitor | ||
| + | [[1u9w]] - hMCTSK+imidazole inhibitor | ||
| + | [[2ftd]] – MCTSK+azepan inhibitor – Macaca mulatta | ||
| + | [[2f7d]] – MCTSK (mutant)+nitrile inhibitor - rabbit | ||
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| + | === Cathepsin-L mature === | ||
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| + | [[3f75]] – MCTSL +CTSL propeptide – Toxoplasma gondii | ||
| + | [[2p86]] – TbMCTSL +K11002 | ||
| + | [[2nqd]] - CTSL residues 1-220 (mutant)+chagasin – Trypanosoma cruzi | ||
| + | [[1mhw]] – hMCTSL +tripeptide | ||
| + | [[1icf]] – hMCTSL +MHC class II fragment | ||
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| + | === Procathepsin-L1 === | ||
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| + | [[2o6x]] – hPCTSL1 (mutant) – Fasciola hepatica | ||
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| + | === Cathepsin-L1 mature === | ||
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| + | [[3iv2]] – hMCTSL1 (mutant) | ||
| + | [[3k24]] - hMCTSL1 (mutant) +tripeptide | ||
| + | [[3bc3]] - hMCTSL1 +inhibitor | ||
| + | [[3h89]], [[3h8b]], [[3h8c]] - hMCTSL1 (mutant) + retro-binding inhibitor | ||
| + | [[3hwn]], [[3hha]] – hMCTSL1+pyrazole inhibitor | ||
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| + | === Cathepsin-L2 mature === | ||
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| + | [[3h6s]] – hMCTSL2+clitocypin | ||
| + | [[1fh0]] – hMCTSL2 (mutant) +vinyl sulfone inhibitor | ||
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| + | === Procathepsin-S === | ||
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| + | [[2c0y]] – hPCTSS (mutant) | ||
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| + | === Cathepsin-S mature === | ||
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| + | [[3n3g]] - hMCTSS+ pyrimidine inhibitor | ||
| + | [[3kwn]] – hMCTSS (mutant)+ thioether acetamide | ||
| + | [[3iej]] - hMCTSS (mutant)+pyrazole inhibitor | ||
| + | [[2h7j]], [[2hxz]]- hMCTSS+triazole inhibitor | ||
| + | [[2r9m]], [[2r9n]], [[2r9o]] – hMCTSS+piperidine inhibitor | ||
| + | [[2op3]], [[2hhn]], [[2g7y]], [[2hh5]], [[2f1g]] – hMCTSS+aryl inhibitor | ||
| + | [[2fud]], [[2fra]], [[2frq]], [[2ft2]], [[1npz]], [[1nqc]] – hMCTSS+inhibitor | ||
| + | [[2fye]], [[2g6d]] – hMCTSS (mutant)+inhibitor | ||
| + | [[2fq9]], [[1ms6]] – hMCTSS +nitrile inhibitor | ||
| + | [[1glo]] - hMCTSS (mutant) | ||
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| + | === Procathepsin-X === | ||
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| + | [[1deu]] - hPCTSX | ||
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| + | === Cathepsin-X mature === | ||
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| + | [[1ef7]] – hMCTSX | ||
Revision as of 07:08, 13 October 2010
Cathepsin (CTS) is a protease which becomes activated at low pH. It is found in lysosomes. Members of the CTS group are denoted as CTSA, CTSB etc and cleave proteins at different peptide bonds. The CTSs are expressed as an inactive precursor pro-CTS (PCTS) which become active when a long residue prosegment is cleaved off producing the mature CTS (MCTS). The images at the left and at the right correspond to one representative Cathepsin, i.e. the crystal structure of wild-type human procathepsin B (1pbh).
3D Structures of Cathepsin
Procathepsin-B
1pbh, 2pbh, 3pbh – hPCTSB - human
Cathepsin-B mature
3hhi – TbCTSB (mutant) residues 23-340+CA074 – Trypanosoma brucei 3k9m – hMCTSB+stefin A 2ipp, 1huc – hMCTSB 3cbj, 3cbk – hMCTSB (mutant)+chagasin 2dc6, 2dc7, 2dc8, 2dc9, 2dca, 2dcb, 2dcc, 2dcd – bMCTSB+inhibitor – bovine 1sp4, 1csb – bMCTSB+epoxysuccinyl inhibitor 1ito, 1qdq – bMCTSB +inhibitor 1gmy - bMCTSB +dipeptidyl nitrile 1the – rMCTSB (mutant)+butanone inhibitor – rat 1cpj - rMCTSB (mutant) 1cte - rMCTSB+pyrimidine inhibitor
Cathepsin-C mature
2djf, 2djg – hMCTSC +Gly-Phe-CHN2 1jqp – rMCTSC 1k3b – hMCTSC
Cathepsin-D mature
1lyw, 1lya – hMCTSD 1lyb - hMCTSD+pepstatin
Cathepsin-E mature
1tzs – hMCTSE+activation peptide from CTSE
Cathepsin-F mature
1m6d – hMCTSF+piperidine inhibitor
Cathepsin-G mature
1kyn – hMCTSG +naphthalene inhibitor 1au8, 1cgh - hMCTSG +phosphonate inhibitor
Cathepsin-H mature
1nb3, 1nb5 – pMCTSH +stefin A – pig 8pch - pMCTSH
Cathepsin-K mature
3o1g, 3n3g, 2r6n, 1bgo, 3kwz, 3kx1 – hMCTSK+ pyrimidine inhibitor 3mpe, 3mpf – hMCTSK (mutant) + pyrimidine inhibitor 3h7d - hMCTSK (mutant) + chondroitin-4-sulfate 3c9e - hMCTSK + chondroitin-4-sulfate 3kwb - hMCTSK (mutant)+dioxo-triazine 3kw9 - hMCTSK +triazine 1yk8 - hMCTSK + cyanamide inhibitor 1yt7 - hMCTSK + ketoamide inhibitor 2aux, 2auz - hMCTSK + semicarbazone inhibitor 1ayu, 1ayv, 1ayw - hMCTSK + carbohydrazide inhibitor 2bdl, 1yk7, 1tu6, 1au3, 1au4 - hMCTSK + pyrrolidine inhibitor 1snk - hMCTSK + norleucine inhibitor 1nl6, 1nlj - hMCTSK+ azepanone inhibitor 1q6k - hMCTSK+carbamate inhibitor 1au0 - hMCTSK+ diacylaminoethyl ketone inhibitor 1au2 - hMCTSK+ propanone inhibitor 1atk – hMCTSK+guanidine inhibitor 1vsn - hMCTSK+ inhibitor 2ato – hMCTSK+myocrisin 1u9v, 1u9x, 1mem – hMCTSK+piperazine inhibitor 1u9w - hMCTSK+imidazole inhibitor 2ftd – MCTSK+azepan inhibitor – Macaca mulatta 2f7d – MCTSK (mutant)+nitrile inhibitor - rabbit
Cathepsin-L mature
3f75 – MCTSL +CTSL propeptide – Toxoplasma gondii 2p86 – TbMCTSL +K11002 2nqd - CTSL residues 1-220 (mutant)+chagasin – Trypanosoma cruzi 1mhw – hMCTSL +tripeptide 1icf – hMCTSL +MHC class II fragment
Procathepsin-L1
2o6x – hPCTSL1 (mutant) – Fasciola hepatica
Cathepsin-L1 mature
3iv2 – hMCTSL1 (mutant) 3k24 - hMCTSL1 (mutant) +tripeptide 3bc3 - hMCTSL1 +inhibitor 3h89, 3h8b, 3h8c - hMCTSL1 (mutant) + retro-binding inhibitor 3hwn, 3hha – hMCTSL1+pyrazole inhibitor
Cathepsin-L2 mature
3h6s – hMCTSL2+clitocypin 1fh0 – hMCTSL2 (mutant) +vinyl sulfone inhibitor
Procathepsin-S
2c0y – hPCTSS (mutant)
Cathepsin-S mature
3n3g - hMCTSS+ pyrimidine inhibitor 3kwn – hMCTSS (mutant)+ thioether acetamide 3iej - hMCTSS (mutant)+pyrazole inhibitor 2h7j, 2hxz- hMCTSS+triazole inhibitor 2r9m, 2r9n, 2r9o – hMCTSS+piperidine inhibitor 2op3, 2hhn, 2g7y, 2hh5, 2f1g – hMCTSS+aryl inhibitor 2fud, 2fra, 2frq, 2ft2, 1npz, 1nqc – hMCTSS+inhibitor 2fye, 2g6d – hMCTSS (mutant)+inhibitor 2fq9, 1ms6 – hMCTSS +nitrile inhibitor 1glo - hMCTSS (mutant)
Procathepsin-X
1deu - hPCTSX
Cathepsin-X mature
1ef7 – hMCTSX
