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: 15 |
NetGPI | no | yes: 0, no: 15 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005739 | mitochondrion | 5 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: A4ICP6
Term | Name | Level | Count |
---|---|---|---|
GO:0006790 | sulfur compound metabolic process | 3 | 16 |
GO:0008152 | metabolic process | 1 | 16 |
GO:0009987 | cellular process | 1 | 16 |
GO:0016043 | cellular component organization | 3 | 16 |
GO:0016226 | iron-sulfur cluster assembly | 4 | 16 |
GO:0022607 | cellular component assembly | 4 | 16 |
GO:0031163 | metallo-sulfur cluster assembly | 5 | 16 |
GO:0044237 | cellular metabolic process | 2 | 16 |
GO:0071840 | cellular component organization or biogenesis | 2 | 16 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0019538 | protein metabolic process | 3 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0051604 | protein maturation | 4 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:0097428 | protein maturation by iron-sulfur cluster transfer | 5 | 2 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 16 |
GO:0005506 | iron ion binding | 6 | 16 |
GO:0043167 | ion binding | 2 | 16 |
GO:0043169 | cation binding | 3 | 16 |
GO:0046872 | metal ion binding | 4 | 16 |
GO:0046914 | transition metal ion binding | 5 | 16 |
GO:0051536 | iron-sulfur cluster binding | 3 | 16 |
GO:0051540 | metal cluster binding | 2 | 16 |
GO:0051539 | 4 iron, 4 sulfur cluster binding | 4 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 163 | 167 | PF00656 | 0.339 |
CLV_C14_Caspase3-7 | 223 | 227 | PF00656 | 0.465 |
CLV_NRD_NRD_1 | 21 | 23 | PF00675 | 0.653 |
CLV_NRD_NRD_1 | 24 | 26 | PF00675 | 0.389 |
CLV_NRD_NRD_1 | 42 | 44 | PF00675 | 0.506 |
CLV_NRD_NRD_1 | 47 | 49 | PF00675 | 0.502 |
CLV_PCSK_KEX2_1 | 21 | 23 | PF00082 | 0.653 |
CLV_PCSK_KEX2_1 | 42 | 44 | PF00082 | 0.526 |
CLV_PCSK_KEX2_1 | 47 | 49 | PF00082 | 0.519 |
CLV_PCSK_PC7_1 | 43 | 49 | PF00082 | 0.610 |
CLV_PCSK_SKI1_1 | 176 | 180 | PF00082 | 0.288 |
CLV_PCSK_SKI1_1 | 230 | 234 | PF00082 | 0.247 |
CLV_PCSK_SKI1_1 | 262 | 266 | PF00082 | 0.436 |
CLV_Separin_Metazoa | 177 | 181 | PF03568 | 0.447 |
DEG_APCC_DBOX_1 | 279 | 287 | PF00400 | 0.607 |
DOC_CKS1_1 | 55 | 60 | PF01111 | 0.318 |
DOC_CYCLIN_RxL_1 | 173 | 181 | PF00134 | 0.350 |
DOC_MAPK_gen_1 | 25 | 35 | PF00069 | 0.416 |
DOC_MAPK_gen_1 | 280 | 288 | PF00069 | 0.499 |
DOC_MAPK_MEF2A_6 | 202 | 210 | PF00069 | 0.465 |
DOC_MAPK_MEF2A_6 | 29 | 37 | PF00069 | 0.572 |
DOC_PP1_RVXF_1 | 127 | 133 | PF00149 | 0.352 |
DOC_PP1_RVXF_1 | 193 | 200 | PF00149 | 0.433 |
DOC_PP1_RVXF_1 | 85 | 92 | PF00149 | 0.318 |
DOC_PP4_FxxP_1 | 111 | 114 | PF00568 | 0.293 |
DOC_PP4_FxxP_1 | 65 | 68 | PF00568 | 0.299 |
DOC_USP7_MATH_1 | 10 | 14 | PF00917 | 0.477 |
DOC_USP7_MATH_1 | 68 | 72 | PF00917 | 0.356 |
DOC_USP7_MATH_2 | 104 | 110 | PF00917 | 0.315 |
DOC_USP7_UBL2_3 | 262 | 266 | PF12436 | 0.486 |
DOC_WW_Pin1_4 | 147 | 152 | PF00397 | 0.384 |
DOC_WW_Pin1_4 | 281 | 286 | PF00397 | 0.586 |
DOC_WW_Pin1_4 | 54 | 59 | PF00397 | 0.315 |
LIG_14-3-3_CanoR_1 | 42 | 46 | PF00244 | 0.499 |
LIG_Actin_WH2_2 | 11 | 27 | PF00022 | 0.411 |
LIG_deltaCOP1_diTrp_1 | 126 | 132 | PF00928 | 0.278 |
LIG_eIF4E_1 | 251 | 257 | PF01652 | 0.420 |
LIG_FHA_1 | 201 | 207 | PF00498 | 0.463 |
LIG_FHA_1 | 238 | 244 | PF00498 | 0.465 |
LIG_FHA_1 | 282 | 288 | PF00498 | 0.515 |
LIG_FHA_2 | 121 | 127 | PF00498 | 0.437 |
LIG_FHA_2 | 154 | 160 | PF00498 | 0.478 |
LIG_FHA_2 | 221 | 227 | PF00498 | 0.438 |
LIG_LIR_Apic_2 | 109 | 114 | PF02991 | 0.270 |
LIG_LIR_Apic_2 | 13 | 19 | PF02991 | 0.412 |
LIG_LIR_Apic_2 | 64 | 68 | PF02991 | 0.368 |
LIG_LIR_Gen_1 | 120 | 130 | PF02991 | 0.319 |
LIG_LIR_Gen_1 | 154 | 162 | PF02991 | 0.419 |
LIG_LIR_Gen_1 | 289 | 296 | PF02991 | 0.515 |
LIG_LIR_Gen_1 | 70 | 77 | PF02991 | 0.313 |
LIG_LIR_Nem_3 | 120 | 125 | PF02991 | 0.314 |
LIG_LIR_Nem_3 | 126 | 130 | PF02991 | 0.293 |
LIG_LIR_Nem_3 | 154 | 158 | PF02991 | 0.371 |
LIG_LIR_Nem_3 | 252 | 257 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 289 | 293 | PF02991 | 0.514 |
LIG_LIR_Nem_3 | 70 | 75 | PF02991 | 0.294 |
LIG_SH2_CRK | 254 | 258 | PF00017 | 0.441 |
LIG_SH2_CRK | 290 | 294 | PF00017 | 0.572 |
LIG_SH2_GRB2like | 122 | 125 | PF00017 | 0.302 |
LIG_SH2_NCK_1 | 122 | 126 | PF00017 | 0.302 |
LIG_SH2_NCK_1 | 155 | 159 | PF00017 | 0.359 |
LIG_SH2_STAT5 | 122 | 125 | PF00017 | 0.392 |
LIG_SH2_STAT5 | 141 | 144 | PF00017 | 0.198 |
LIG_SH2_STAT5 | 155 | 158 | PF00017 | 0.313 |
LIG_SH3_3 | 2 | 8 | PF00018 | 0.546 |
LIG_TYR_ITIM | 288 | 293 | PF00017 | 0.601 |
LIG_WRC_WIRS_1 | 134 | 139 | PF05994 | 0.273 |
LIG_WRC_WIRS_1 | 72 | 77 | PF05994 | 0.402 |
MOD_CDC14_SPxK_1 | 150 | 153 | PF00782 | 0.399 |
MOD_CDK_SPxK_1 | 147 | 153 | PF00069 | 0.394 |
MOD_CK1_1 | 120 | 126 | PF00069 | 0.363 |
MOD_CK1_1 | 133 | 139 | PF00069 | 0.199 |
MOD_CK1_1 | 220 | 226 | PF00069 | 0.457 |
MOD_CK1_1 | 71 | 77 | PF00069 | 0.441 |
MOD_CK2_1 | 125 | 131 | PF00069 | 0.361 |
MOD_CK2_1 | 153 | 159 | PF00069 | 0.451 |
MOD_CK2_1 | 164 | 170 | PF00069 | 0.399 |
MOD_GSK3_1 | 200 | 207 | PF00069 | 0.446 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.486 |
MOD_N-GLC_2 | 146 | 148 | PF02516 | 0.384 |
MOD_NEK2_1 | 142 | 147 | PF00069 | 0.399 |
MOD_NEK2_1 | 36 | 41 | PF00069 | 0.492 |
MOD_NEK2_1 | 61 | 66 | PF00069 | 0.399 |
MOD_PIKK_1 | 217 | 223 | PF00454 | 0.447 |
MOD_PIKK_1 | 93 | 99 | PF00454 | 0.346 |
MOD_PK_1 | 115 | 121 | PF00069 | 0.293 |
MOD_PKA_2 | 41 | 47 | PF00069 | 0.471 |
MOD_Plk_1 | 130 | 136 | PF00069 | 0.273 |
MOD_Plk_1 | 153 | 159 | PF00069 | 0.462 |
MOD_Plk_4 | 10 | 16 | PF00069 | 0.670 |
MOD_Plk_4 | 106 | 112 | PF00069 | 0.270 |
MOD_Plk_4 | 133 | 139 | PF00069 | 0.263 |
MOD_Plk_4 | 153 | 159 | PF00069 | 0.253 |
MOD_Plk_4 | 36 | 42 | PF00069 | 0.587 |
MOD_Plk_4 | 71 | 77 | PF00069 | 0.391 |
MOD_ProDKin_1 | 147 | 153 | PF00069 | 0.394 |
MOD_ProDKin_1 | 281 | 287 | PF00069 | 0.585 |
MOD_ProDKin_1 | 54 | 60 | PF00069 | 0.315 |
MOD_SUMO_rev_2 | 159 | 167 | PF00179 | 0.412 |
MOD_SUMO_rev_2 | 190 | 197 | PF00179 | 0.430 |
TRG_DiLeu_BaEn_1 | 252 | 257 | PF01217 | 0.428 |
TRG_ENDOCYTIC_2 | 122 | 125 | PF00928 | 0.347 |
TRG_ENDOCYTIC_2 | 141 | 144 | PF00928 | 0.205 |
TRG_ENDOCYTIC_2 | 155 | 158 | PF00928 | 0.311 |
TRG_ENDOCYTIC_2 | 254 | 257 | PF00928 | 0.396 |
TRG_ENDOCYTIC_2 | 290 | 293 | PF00928 | 0.549 |
TRG_ER_diArg_1 | 20 | 22 | PF00400 | 0.655 |
TRG_ER_diArg_1 | 41 | 43 | PF00400 | 0.534 |
TRG_ER_diArg_1 | 47 | 49 | PF00400 | 0.521 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I2Q0 | Leptomonas seymouri | 35% | 100% |
A0A0N1I735 | Leptomonas seymouri | 82% | 100% |
A0A0S4IJH0 | Bodo saltans | 33% | 100% |
A0A0S4IVB5 | Bodo saltans | 58% | 100% |
A0A1X0NST9 | Trypanosomatidae | 33% | 100% |
A0A1X0P8F8 | Trypanosomatidae | 67% | 100% |
A0A3S5H7F5 | Leishmania donovani | 34% | 100% |
A0A3S7XAI2 | Leishmania donovani | 99% | 100% |
A4HEM5 | Leishmania braziliensis | 34% | 100% |
A4HNU8 | Leishmania braziliensis | 92% | 100% |
A4I1V6 | Leishmania infantum | 34% | 100% |
B3MRT7 | Drosophila ananassae | 29% | 100% |
B3NYF7 | Drosophila erecta | 29% | 100% |
B4H303 | Drosophila persimilis | 29% | 100% |
B4IMF6 | Drosophila sechellia | 28% | 100% |
B4JWR9 | Drosophila grimshawi | 27% | 100% |
B4M375 | Drosophila virilis | 29% | 100% |
B4NE93 | Drosophila willistoni | 29% | 100% |
B4PZ52 | Drosophila yakuba | 30% | 100% |
B4R3T1 | Drosophila simulans | 30% | 100% |
B5DKJ8 | Drosophila pseudoobscura pseudoobscura | 29% | 100% |
C9ZS65 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
D0A2R6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 69% | 100% |
E9ASK8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
E9AY01 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 100% |
P32860 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 29% | 100% |
Q4Q1Y8 | Leishmania major | 95% | 100% |
Q4Q9H2 | Leishmania major | 34% | 100% |
Q8SY96 | Drosophila melanogaster | 28% | 100% |
Q9C8J2 | Arabidopsis thaliana | 33% | 100% |
Q9LIG6 | Arabidopsis thaliana | 32% | 100% |
Q9QZ23 | Mus musculus | 33% | 100% |
V5DRN0 | Trypanosoma cruzi | 73% | 100% |