This cluster contains a high variety of cytochrome b5 homologs. Although all membrane-anchored, some use the N-terminal [type-III] while others the C-terminal TM helix [type-IV]. The heme domain is assumed to be cytoplasmic.. Localization: ER (by homology) / Mitochondrial outer membrane (by homology)
Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 5 |
NetGPI | no | yes: 0, no: 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 3 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
Related structures:
AlphaFold database: A4H991
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 4 |
GO:0020037 | heme binding | 4 | 4 |
GO:0043167 | ion binding | 2 | 4 |
GO:0043169 | cation binding | 3 | 4 |
GO:0046872 | metal ion binding | 4 | 4 |
GO:0046906 | tetrapyrrole binding | 3 | 4 |
GO:0097159 | organic cyclic compound binding | 2 | 4 |
GO:1901363 | heterocyclic compound binding | 2 | 4 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_PCSK_SKI1_1 | 215 | 219 | PF00082 | 0.705 |
DEG_SPOP_SBC_1 | 2 | 6 | PF00917 | 0.634 |
DOC_MAPK_MEF2A_6 | 154 | 163 | PF00069 | 0.433 |
DOC_MAPK_MEF2A_6 | 49 | 57 | PF00069 | 0.339 |
DOC_PP1_RVXF_1 | 26 | 33 | PF00149 | 0.622 |
DOC_PP4_FxxP_1 | 199 | 202 | PF00568 | 0.320 |
DOC_USP7_MATH_1 | 2 | 6 | PF00917 | 0.634 |
DOC_USP7_MATH_1 | 7 | 11 | PF00917 | 0.625 |
DOC_USP7_MATH_1 | 94 | 98 | PF00917 | 0.635 |
DOC_USP7_UBL2_3 | 21 | 25 | PF12436 | 0.639 |
DOC_WW_Pin1_4 | 103 | 108 | PF00397 | 0.539 |
DOC_WW_Pin1_4 | 13 | 18 | PF00397 | 0.653 |
DOC_WW_Pin1_4 | 3 | 8 | PF00397 | 0.632 |
DOC_WW_Pin1_4 | 96 | 101 | PF00397 | 0.613 |
LIG_14-3-3_CanoR_1 | 144 | 150 | PF00244 | 0.433 |
LIG_14-3-3_CanoR_1 | 19 | 25 | PF00244 | 0.694 |
LIG_14-3-3_CanoR_1 | 28 | 33 | PF00244 | 0.596 |
LIG_14-3-3_CanoR_1 | 71 | 76 | PF00244 | 0.429 |
LIG_APCC_ABBA_1 | 109 | 114 | PF00400 | 0.420 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.644 |
LIG_BRCT_BRCA1_1 | 71 | 75 | PF00533 | 0.411 |
LIG_EH1_1 | 210 | 218 | PF00400 | 0.400 |
LIG_FHA_1 | 104 | 110 | PF00498 | 0.607 |
LIG_FHA_1 | 25 | 31 | PF00498 | 0.621 |
LIG_FHA_2 | 144 | 150 | PF00498 | 0.352 |
LIG_FHA_2 | 153 | 159 | PF00498 | 0.287 |
LIG_Integrin_isoDGR_2 | 47 | 49 | PF01839 | 0.383 |
LIG_LIR_Gen_1 | 157 | 168 | PF02991 | 0.433 |
LIG_LIR_Gen_1 | 194 | 202 | PF02991 | 0.347 |
LIG_LIR_Gen_1 | 31 | 41 | PF02991 | 0.621 |
LIG_LIR_Gen_1 | 72 | 81 | PF02991 | 0.420 |
LIG_LIR_Nem_3 | 157 | 163 | PF02991 | 0.433 |
LIG_LIR_Nem_3 | 194 | 199 | PF02991 | 0.347 |
LIG_LIR_Nem_3 | 31 | 36 | PF02991 | 0.621 |
LIG_LIR_Nem_3 | 72 | 76 | PF02991 | 0.425 |
LIG_PCNA_PIPBox_1 | 192 | 201 | PF02747 | 0.433 |
LIG_PCNA_PIPBox_1 | 26 | 35 | PF02747 | 0.620 |
LIG_PCNA_yPIPBox_3 | 19 | 33 | PF02747 | 0.632 |
LIG_SH2_NCK_1 | 131 | 135 | PF00017 | 0.329 |
LIG_SH2_STAP1 | 126 | 130 | PF00017 | 0.466 |
LIG_SH2_STAT5 | 145 | 148 | PF00017 | 0.324 |
LIG_SH3_3 | 172 | 178 | PF00018 | 0.433 |
LIG_SH3_3 | 73 | 79 | PF00018 | 0.518 |
LIG_Sin3_3 | 54 | 61 | PF02671 | 0.339 |
LIG_TRAF2_1 | 146 | 149 | PF00917 | 0.433 |
LIG_WRC_WIRS_1 | 29 | 34 | PF05994 | 0.621 |
LIG_WRC_WIRS_1 | 70 | 75 | PF05994 | 0.492 |
MOD_CDC14_SPxK_1 | 16 | 19 | PF00782 | 0.652 |
MOD_CDK_SPxK_1 | 13 | 19 | PF00069 | 0.657 |
MOD_CK1_1 | 31 | 37 | PF00069 | 0.623 |
MOD_CK2_1 | 143 | 149 | PF00069 | 0.352 |
MOD_GlcNHglycan | 170 | 173 | PF01048 | 0.633 |
MOD_GlcNHglycan | 96 | 99 | PF01048 | 0.697 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.623 |
MOD_GSK3_1 | 24 | 31 | PF00069 | 0.585 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.636 |
MOD_GSK3_1 | 96 | 103 | PF00069 | 0.598 |
MOD_N-GLC_1 | 168 | 173 | PF02516 | 0.615 |
MOD_N-GLC_2 | 210 | 212 | PF02516 | 0.466 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.641 |
MOD_NEK2_1 | 130 | 135 | PF00069 | 0.328 |
MOD_NEK2_1 | 168 | 173 | PF00069 | 0.433 |
MOD_NEK2_1 | 24 | 29 | PF00069 | 0.583 |
MOD_NEK2_1 | 8 | 13 | PF00069 | 0.627 |
MOD_PIKK_1 | 143 | 149 | PF00454 | 0.352 |
MOD_PIKK_1 | 152 | 158 | PF00454 | 0.287 |
MOD_PKA_2 | 143 | 149 | PF00069 | 0.433 |
MOD_PKA_2 | 94 | 100 | PF00069 | 0.467 |
MOD_Plk_1 | 168 | 174 | PF00069 | 0.415 |
MOD_Plk_4 | 191 | 197 | PF00069 | 0.334 |
MOD_Plk_4 | 28 | 34 | PF00069 | 0.622 |
MOD_ProDKin_1 | 103 | 109 | PF00069 | 0.538 |
MOD_ProDKin_1 | 13 | 19 | PF00069 | 0.653 |
MOD_ProDKin_1 | 3 | 9 | PF00069 | 0.634 |
MOD_ProDKin_1 | 96 | 102 | PF00069 | 0.612 |
TRG_DiLeu_BaLyEn_6 | 203 | 208 | PF01217 | 0.308 |
TRG_ER_diArg_1 | 36 | 39 | PF00400 | 0.622 |
TRG_Pf-PMV_PEXEL_1 | 215 | 219 | PF00026 | 0.705 |
TRG_Pf-PMV_PEXEL_1 | 39 | 43 | PF00026 | 0.418 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7WUN9 | Leishmania donovani | 60% | 100% |
A4HXL2 | Leishmania infantum | 60% | 100% |
E9ARA8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 63% | 100% |
Q4QE55 | Leishmania major | 60% | 100% |