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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005739 | mitochondrion | 5 | 1 |
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 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4H8K7
Term | Name | Level | Count |
---|---|---|---|
GO:0006790 | sulfur compound metabolic process | 3 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016043 | cellular component organization | 3 | 12 |
GO:0016226 | iron-sulfur cluster assembly | 4 | 12 |
GO:0022607 | cellular component assembly | 4 | 12 |
GO:0031163 | metallo-sulfur cluster assembly | 5 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0071840 | cellular component organization or biogenesis | 2 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0051604 | protein maturation | 4 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0097428 | protein maturation by iron-sulfur cluster transfer | 5 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 12 |
GO:0051536 | iron-sulfur cluster binding | 3 | 12 |
GO:0051540 | metal cluster binding | 2 | 12 |
GO:0051537 | 2 iron, 2 sulfur cluster binding | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 68 | 72 | PF00656 | 0.609 |
CLV_NRD_NRD_1 | 102 | 104 | PF00675 | 0.511 |
CLV_NRD_NRD_1 | 110 | 112 | PF00675 | 0.413 |
CLV_NRD_NRD_1 | 129 | 131 | PF00675 | 0.480 |
CLV_NRD_NRD_1 | 169 | 171 | PF00675 | 0.275 |
CLV_NRD_NRD_1 | 196 | 198 | PF00675 | 0.301 |
CLV_PCSK_KEX2_1 | 110 | 112 | PF00082 | 0.479 |
CLV_PCSK_KEX2_1 | 129 | 131 | PF00082 | 0.366 |
CLV_PCSK_KEX2_1 | 168 | 170 | PF00082 | 0.242 |
CLV_PCSK_KEX2_1 | 187 | 189 | PF00082 | 0.355 |
CLV_PCSK_PC1ET2_1 | 187 | 189 | PF00082 | 0.369 |
CLV_PCSK_PC7_1 | 164 | 170 | PF00082 | 0.264 |
CLV_PCSK_SKI1_1 | 118 | 122 | PF00082 | 0.445 |
CLV_PCSK_SKI1_1 | 129 | 133 | PF00082 | 0.444 |
CLV_PCSK_SKI1_1 | 191 | 195 | PF00082 | 0.279 |
DEG_SPOP_SBC_1 | 72 | 76 | PF00917 | 0.776 |
DOC_CYCLIN_RxL_1 | 129 | 139 | PF00134 | 0.516 |
DOC_PP1_RVXF_1 | 109 | 116 | PF00149 | 0.530 |
DOC_PP4_FxxP_1 | 243 | 246 | PF00568 | 0.439 |
DOC_USP7_MATH_1 | 150 | 154 | PF00917 | 0.683 |
DOC_USP7_MATH_1 | 158 | 162 | PF00917 | 0.502 |
DOC_USP7_MATH_1 | 18 | 22 | PF00917 | 0.728 |
DOC_USP7_MATH_1 | 23 | 27 | PF00917 | 0.711 |
DOC_USP7_MATH_1 | 89 | 93 | PF00917 | 0.654 |
DOC_USP7_UBL2_3 | 187 | 191 | PF12436 | 0.463 |
DOC_USP7_UBL2_3 | 240 | 244 | PF12436 | 0.497 |
DOC_USP7_UBL2_3 | 40 | 44 | PF12436 | 0.622 |
DOC_WW_Pin1_4 | 103 | 108 | PF00397 | 0.501 |
DOC_WW_Pin1_4 | 121 | 126 | PF00397 | 0.451 |
DOC_WW_Pin1_4 | 146 | 151 | PF00397 | 0.678 |
DOC_WW_Pin1_4 | 191 | 196 | PF00397 | 0.537 |
DOC_WW_Pin1_4 | 46 | 51 | PF00397 | 0.734 |
DOC_WW_Pin1_4 | 81 | 86 | PF00397 | 0.666 |
LIG_14-3-3_CanoR_1 | 90 | 100 | PF00244 | 0.594 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.497 |
LIG_BRCT_BRCA1_1 | 83 | 87 | PF00533 | 0.558 |
LIG_FHA_1 | 33 | 39 | PF00498 | 0.617 |
LIG_FHA_1 | 46 | 52 | PF00498 | 0.502 |
LIG_FHA_1 | 7 | 13 | PF00498 | 0.662 |
LIG_FHA_2 | 226 | 232 | PF00498 | 0.439 |
LIG_FHA_2 | 233 | 239 | PF00498 | 0.548 |
LIG_FHA_2 | 74 | 80 | PF00498 | 0.513 |
LIG_Integrin_RGD_1 | 188 | 190 | PF01839 | 0.180 |
LIG_LIR_Apic_2 | 242 | 246 | PF02991 | 0.439 |
LIG_LIR_LC3C_4 | 205 | 208 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 220 | 226 | PF02991 | 0.501 |
LIG_LIR_Nem_3 | 256 | 261 | PF02991 | 0.389 |
LIG_SH2_SRC | 224 | 227 | PF00017 | 0.439 |
LIG_SH2_STAP1 | 175 | 179 | PF00017 | 0.439 |
LIG_SH2_STAT5 | 177 | 180 | PF00017 | 0.439 |
LIG_SH2_STAT5 | 182 | 185 | PF00017 | 0.439 |
LIG_SH2_STAT5 | 224 | 227 | PF00017 | 0.456 |
LIG_SH2_STAT5 | 232 | 235 | PF00017 | 0.450 |
LIG_SH3_3 | 144 | 150 | PF00018 | 0.542 |
LIG_SH3_3 | 9 | 15 | PF00018 | 0.638 |
LIG_TRAF2_1 | 54 | 57 | PF00917 | 0.498 |
LIG_TRFH_1 | 121 | 125 | PF08558 | 0.370 |
LIG_WW_3 | 194 | 198 | PF00397 | 0.195 |
MOD_CDK_SPxK_1 | 191 | 197 | PF00069 | 0.390 |
MOD_CDK_SPxxK_3 | 103 | 110 | PF00069 | 0.488 |
MOD_CDK_SPxxK_3 | 191 | 198 | PF00069 | 0.357 |
MOD_CDK_SPxxK_3 | 46 | 53 | PF00069 | 0.642 |
MOD_CK1_1 | 149 | 155 | PF00069 | 0.667 |
MOD_CK1_1 | 16 | 22 | PF00069 | 0.731 |
MOD_CK1_1 | 173 | 179 | PF00069 | 0.239 |
MOD_CK1_1 | 26 | 32 | PF00069 | 0.666 |
MOD_CK1_1 | 91 | 97 | PF00069 | 0.588 |
MOD_CK2_1 | 1 | 7 | PF00069 | 0.492 |
MOD_CK2_1 | 232 | 238 | PF00069 | 0.373 |
MOD_CK2_1 | 51 | 57 | PF00069 | 0.657 |
MOD_CK2_1 | 73 | 79 | PF00069 | 0.512 |
MOD_CK2_1 | 89 | 95 | PF00069 | 0.529 |
MOD_GlcNHglycan | 142 | 145 | PF01048 | 0.647 |
MOD_GlcNHglycan | 154 | 158 | PF01048 | 0.516 |
MOD_GlcNHglycan | 160 | 163 | PF01048 | 0.358 |
MOD_GlcNHglycan | 172 | 175 | PF01048 | 0.243 |
MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.298 |
MOD_GlcNHglycan | 20 | 23 | PF01048 | 0.727 |
MOD_GlcNHglycan | 25 | 28 | PF01048 | 0.732 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.680 |
MOD_GSK3_1 | 136 | 143 | PF00069 | 0.567 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.647 |
MOD_NEK2_1 | 38 | 43 | PF00069 | 0.692 |
MOD_PIKK_1 | 32 | 38 | PF00454 | 0.636 |
MOD_PKA_2 | 16 | 22 | PF00069 | 0.764 |
MOD_PKA_2 | 89 | 95 | PF00069 | 0.593 |
MOD_PKB_1 | 168 | 176 | PF00069 | 0.312 |
MOD_Plk_4 | 225 | 231 | PF00069 | 0.195 |
MOD_Plk_4 | 254 | 260 | PF00069 | 0.388 |
MOD_ProDKin_1 | 103 | 109 | PF00069 | 0.498 |
MOD_ProDKin_1 | 121 | 127 | PF00069 | 0.444 |
MOD_ProDKin_1 | 146 | 152 | PF00069 | 0.679 |
MOD_ProDKin_1 | 191 | 197 | PF00069 | 0.414 |
MOD_ProDKin_1 | 46 | 52 | PF00069 | 0.735 |
MOD_ProDKin_1 | 81 | 87 | PF00069 | 0.666 |
TRG_ER_diArg_1 | 128 | 130 | PF00400 | 0.382 |
TRG_ER_diArg_1 | 167 | 170 | PF00400 | 0.312 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I6U6 | Leptomonas seymouri | 63% | 100% |
A0A0S4KJP5 | Bodo saltans | 52% | 100% |
A0A1X0NZ22 | Trypanosomatidae | 48% | 100% |
A0A3Q8IAJ0 | Leishmania donovani | 78% | 92% |
A0A422NDJ9 | Trypanosoma rangeli | 52% | 92% |
A4HWY0 | Leishmania infantum | 78% | 92% |
C9ZW24 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 50% | 99% |
E9AQP2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 92% |
Q4QET6 | Leishmania major | 76% | 100% |
V5BHL1 | Trypanosoma cruzi | 47% | 84% |