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: 10 |
NetGPI | no | yes: 0, no: 10 |
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: E9AQP2
Term | Name | Level | Count |
---|---|---|---|
GO:0006790 | sulfur compound metabolic process | 3 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0016043 | cellular component organization | 3 | 11 |
GO:0016226 | iron-sulfur cluster assembly | 4 | 11 |
GO:0022607 | cellular component assembly | 4 | 11 |
GO:0031163 | metallo-sulfur cluster assembly | 5 | 11 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0071840 | cellular component organization or biogenesis | 2 | 11 |
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 | 11 |
GO:0051536 | iron-sulfur cluster binding | 3 | 11 |
GO:0051540 | metal cluster binding | 2 | 11 |
GO:0051537 | 2 iron, 2 sulfur cluster binding | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 91 | 95 | PF00656 | 0.584 |
CLV_NRD_NRD_1 | 152 | 154 | PF00675 | 0.451 |
CLV_NRD_NRD_1 | 17 | 19 | PF00675 | 0.534 |
CLV_NRD_NRD_1 | 192 | 194 | PF00675 | 0.269 |
CLV_NRD_NRD_1 | 219 | 221 | PF00675 | 0.295 |
CLV_PCSK_KEX2_1 | 133 | 135 | PF00082 | 0.457 |
CLV_PCSK_KEX2_1 | 152 | 154 | PF00082 | 0.351 |
CLV_PCSK_KEX2_1 | 17 | 19 | PF00082 | 0.671 |
CLV_PCSK_KEX2_1 | 191 | 193 | PF00082 | 0.246 |
CLV_PCSK_PC1ET2_1 | 133 | 135 | PF00082 | 0.569 |
CLV_PCSK_PC7_1 | 187 | 193 | PF00082 | 0.257 |
CLV_PCSK_SKI1_1 | 141 | 145 | PF00082 | 0.429 |
CLV_PCSK_SKI1_1 | 152 | 156 | PF00082 | 0.420 |
CLV_PCSK_SKI1_1 | 17 | 21 | PF00082 | 0.570 |
DEG_COP1_1 | 175 | 186 | PF00400 | 0.418 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.518 |
DEG_SCF_TRCP1_1 | 43 | 49 | PF00400 | 0.539 |
DEG_SPOP_SBC_1 | 28 | 32 | PF00917 | 0.700 |
DOC_CKS1_1 | 145 | 150 | PF01111 | 0.498 |
DOC_CYCLIN_RxL_1 | 14 | 23 | PF00134 | 0.566 |
DOC_MAPK_RevD_3 | 4 | 18 | PF00069 | 0.414 |
DOC_PP1_RVXF_1 | 132 | 139 | PF00149 | 0.508 |
DOC_PP4_FxxP_1 | 266 | 269 | PF00568 | 0.444 |
DOC_USP7_MATH_1 | 112 | 116 | PF00917 | 0.689 |
DOC_USP7_MATH_1 | 173 | 177 | PF00917 | 0.537 |
DOC_USP7_MATH_1 | 209 | 213 | PF00917 | 0.553 |
DOC_USP7_MATH_1 | 216 | 220 | PF00917 | 0.538 |
DOC_USP7_MATH_1 | 28 | 32 | PF00917 | 0.697 |
DOC_USP7_MATH_1 | 46 | 50 | PF00917 | 0.696 |
DOC_USP7_MATH_1 | 95 | 99 | PF00917 | 0.736 |
DOC_USP7_UBL2_3 | 263 | 267 | PF12436 | 0.501 |
DOC_USP7_UBL2_3 | 63 | 67 | PF12436 | 0.599 |
DOC_WW_Pin1_4 | 126 | 131 | PF00397 | 0.485 |
DOC_WW_Pin1_4 | 144 | 149 | PF00397 | 0.375 |
DOC_WW_Pin1_4 | 214 | 219 | PF00397 | 0.538 |
DOC_WW_Pin1_4 | 69 | 74 | PF00397 | 0.721 |
LIG_14-3-3_CanoR_1 | 113 | 123 | PF00244 | 0.586 |
LIG_BIR_III_2 | 119 | 123 | PF00653 | 0.638 |
LIG_CaM_IQ_9 | 55 | 71 | PF13499 | 0.439 |
LIG_FHA_1 | 1 | 7 | PF00498 | 0.551 |
LIG_FHA_1 | 36 | 42 | PF00498 | 0.642 |
LIG_FHA_1 | 56 | 62 | PF00498 | 0.593 |
LIG_FHA_1 | 69 | 75 | PF00498 | 0.497 |
LIG_FHA_2 | 249 | 255 | PF00498 | 0.444 |
LIG_FHA_2 | 256 | 262 | PF00498 | 0.529 |
LIG_LIR_Apic_2 | 265 | 269 | PF02991 | 0.444 |
LIG_LIR_Apic_2 | 77 | 81 | PF02991 | 0.610 |
LIG_LIR_Nem_3 | 243 | 249 | PF02991 | 0.518 |
LIG_LIR_Nem_3 | 279 | 284 | PF02991 | 0.397 |
LIG_SH2_SRC | 247 | 250 | PF00017 | 0.444 |
LIG_SH2_STAP1 | 198 | 202 | PF00017 | 0.444 |
LIG_SH2_STAT5 | 156 | 159 | PF00017 | 0.354 |
LIG_SH2_STAT5 | 200 | 203 | PF00017 | 0.444 |
LIG_SH2_STAT5 | 247 | 250 | PF00017 | 0.462 |
LIG_SH2_STAT5 | 255 | 258 | PF00017 | 0.444 |
LIG_SH3_3 | 142 | 148 | PF00018 | 0.501 |
LIG_SxIP_EBH_1 | 67 | 79 | PF03271 | 0.596 |
LIG_TRFH_1 | 144 | 148 | PF08558 | 0.355 |
LIG_WRC_WIRS_1 | 1 | 6 | PF05994 | 0.411 |
LIG_WRC_WIRS_1 | 62 | 67 | PF05994 | 0.510 |
MOD_CDK_SPxK_1 | 214 | 220 | PF00069 | 0.520 |
MOD_CDK_SPxxK_3 | 126 | 133 | PF00069 | 0.468 |
MOD_CDK_SPxxK_3 | 214 | 221 | PF00069 | 0.501 |
MOD_CDK_SPxxK_3 | 69 | 76 | PF00069 | 0.640 |
MOD_CK1_1 | 114 | 120 | PF00069 | 0.585 |
MOD_CK1_1 | 176 | 182 | PF00069 | 0.522 |
MOD_CK1_1 | 196 | 202 | PF00069 | 0.417 |
MOD_CK1_1 | 39 | 45 | PF00069 | 0.774 |
MOD_CK1_1 | 49 | 55 | PF00069 | 0.654 |
MOD_CK2_1 | 112 | 118 | PF00069 | 0.545 |
MOD_CK2_1 | 255 | 261 | PF00069 | 0.540 |
MOD_CK2_1 | 74 | 80 | PF00069 | 0.657 |
MOD_GlcNHglycan | 165 | 168 | PF01048 | 0.550 |
MOD_GlcNHglycan | 183 | 186 | PF01048 | 0.204 |
MOD_GlcNHglycan | 195 | 198 | PF01048 | 0.230 |
MOD_GlcNHglycan | 207 | 210 | PF01048 | 0.259 |
MOD_GlcNHglycan | 211 | 214 | PF01048 | 0.269 |
MOD_GlcNHglycan | 43 | 46 | PF01048 | 0.696 |
MOD_GlcNHglycan | 97 | 100 | PF01048 | 0.605 |
MOD_GSK3_1 | 172 | 179 | PF00069 | 0.423 |
MOD_GSK3_1 | 205 | 212 | PF00069 | 0.550 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.707 |
MOD_GSK3_1 | 51 | 58 | PF00069 | 0.549 |
MOD_N-GLC_1 | 36 | 41 | PF02516 | 0.749 |
MOD_NEK2_1 | 19 | 24 | PF00069 | 0.578 |
MOD_NEK2_1 | 41 | 46 | PF00069 | 0.461 |
MOD_NEK2_1 | 51 | 56 | PF00069 | 0.668 |
MOD_NEK2_1 | 61 | 66 | PF00069 | 0.675 |
MOD_PIKK_1 | 55 | 61 | PF00454 | 0.614 |
MOD_PKA_2 | 112 | 118 | PF00069 | 0.593 |
MOD_PKA_2 | 39 | 45 | PF00069 | 0.694 |
MOD_PKA_2 | 68 | 74 | PF00069 | 0.673 |
MOD_PKB_1 | 191 | 199 | PF00069 | 0.457 |
MOD_Plk_1 | 36 | 42 | PF00069 | 0.476 |
MOD_Plk_4 | 277 | 283 | PF00069 | 0.529 |
MOD_Plk_4 | 51 | 57 | PF00069 | 0.518 |
MOD_ProDKin_1 | 126 | 132 | PF00069 | 0.481 |
MOD_ProDKin_1 | 144 | 150 | PF00069 | 0.368 |
MOD_ProDKin_1 | 214 | 220 | PF00069 | 0.538 |
MOD_ProDKin_1 | 69 | 75 | PF00069 | 0.724 |
TRG_DiLeu_BaLyEn_6 | 105 | 110 | PF01217 | 0.482 |
TRG_ENDOCYTIC_2 | 62 | 65 | PF00928 | 0.685 |
TRG_ER_diArg_1 | 151 | 153 | PF00400 | 0.352 |
TRG_ER_diArg_1 | 17 | 19 | PF00400 | 0.534 |
TRG_ER_diArg_1 | 190 | 193 | PF00400 | 0.457 |
TRG_Pf-PMV_PEXEL_1 | 17 | 21 | PF00026 | 0.432 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I6U6 | Leptomonas seymouri | 68% | 100% |
A0A1X0NZ22 | Trypanosomatidae | 58% | 100% |
A0A3Q8IAJ0 | Leishmania donovani | 88% | 100% |
A0A422NDJ9 | Trypanosoma rangeli | 51% | 100% |
A4H8K7 | Leishmania braziliensis | 78% | 100% |
A4HWY0 | Leishmania infantum | 89% | 100% |
C9ZW24 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 49% | 100% |
Q4QET6 | Leishmania major | 85% | 100% |
V5BHL1 | Trypanosoma cruzi | 49% | 91% |