2hod

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PDB ID 2hod

Drag the structure with the mouse to rotate
, resolution 2.9Å
Ligands: , , and
Coordinates: save as pdb, mmCIF, xml



Crystal Structure of Fragment D from Human Fibrinogen Complexed with Gly-hydroxyPro-Arg-Pro-amide


Disease

Known diseases associated with this structure: Afibrinogenemia, congenital OMIM:[134820], Afibrinogenemia, congenital OMIM:[134830], Amyloidosis, hereditary renal OMIM:[134820], Dysfibrinogenemia, alpha type, causing bleeding diathesis OMIM:[134820], Dysfibrinogenemia, alpha type, causing recurrent thrombosis OMIM:[134820], Dysfibrinogenemia, beta type OMIM:[134830], Thrombophilia, dysfibrinogenemic OMIM:[134830]

About this Structure

2HOD is a Protein complex structure of sequences from Homo sapiens. Full crystallographic information is available from OCA.

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