Nibrin (NBN)

Homo sapiens — UniProt O60934

Gene: NBNHomo sapiensSwissProt reviewed

About Nibrin

Nibrin (NBN) is a protein from Homo sapiens identified by UniProt accession O60934, 754 residues long. MolForge cross-references it against 0 known binders and 283 disease associations.

Target properties

Protein nameNibrin
UniProt accessionO60934
GeneNBN
OrganismHomo sapiens
Length754 residues
Molecular weight—
EC numbers—
Target classUNCLASSIFIED
Subcellular location—
Keywords—

Druggability

Target tractability assessment (Open Targets + pocket analysis). No approved drug

Druggability tierMEDIUM
Druggability score—
Pocket score—
Max clinical phase—

Disease associations (283)

Diseases linked to this target (Open Targets).

  • Nijmegen breakage syndrome · score 0.82
  • Aplastic anemia · score 0.73
  • acute lymphoblastic leukemia · score 0.66
  • T-cell acute lymphoblastic leukemia · score 0.61
  • breast carcinoma · score 0.61
  • Inherited cancer-predisposing syndrome · score 0.58
  • hereditary neoplastic syndrome · score 0.58
  • hereditary breast carcinoma · score 0.55
  • Hereditary breast and ovarian cancer syndrome · score 0.54
  • aplastic anemia · score 0.53

3D Structure (1)

Experimental (PDB) and predicted (AlphaFold) structures for this protein.

StructureSourceMethodMean pLDDTResolution (Å)
AF-O60934-F1alphafoldPREDICTED63.09—

Amino-acid sequence (754 residues)

MWKLLPAAGP AGGEPYRLLT GVEYVVGRKN CAILIENDQS ISRNHAVLTA NFSVTNLSQT DEIPVLTLKD NSKYGTFVNE EKMQNGFSRT LKSGDGITFG VFGSKFRIEY EPLVACSSCL DVSGKTALNQ AILQLGGFTV NNWTEECTHL VMVSVKVTIK TICALICGRP IVKPEYFTEF LKAVESKKQP PQIESFYPPL DEPSIGSKNV DLSGRQERKQ IFKGKTFIFL NAKQHKKLSS AVVFGGGEAR LITEENEEEH NFFLAPGTCV VDTGITNSQT LIPDCQKKWI QSIMDMLQRQ GLRPIPEAEI GLAVIFMTTK NYCDPQGHPS TGLKTTTPGP SLSQGVSVDE KLMPSAPVNT TTYVADTESE QADTWDLSER PKEIKVSKME QKFRMLSQDA PTVKESCKTS SNNNSMVSNT LAKMRIPNYQ LSPTKLPSIN KSKDRASQQQ QTNSIRNYFQ PSTKKRERDE ENQEMSSCKS ARIETSCSLL EQTQPATPSL WKNKEQHLSE NEPVDTNSDN NLFTDTDLKS IVKNSASKSH AAEKLRSNKK REMDDVAIED EVLEQLFKDT KPELEIDVKV QKQEEDVNVR KRPRMDIETN DTFSDEAVPE SSKISQENEI GKKRELKEDS LWSAKEISNN DKLQDDSEML PKKLLLTEFR SLVIKNSTSR NPSGINDDYG QLKNFKKFKK VTYPGAGKLP HIIGGSDLIA HHARKNTELE EWLRQEMEVQ NQHAKEESLA DDLFRYNPYL KRRR

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Quick facts

UniProtO60934
GeneNBN
OrganismHomo sapiens
Length754
Binders0
Diseases283
View on UniProt