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: 17 |
NetGPI | no | yes: 0, no: 17 |
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: E9ASK8
Term | Name | Level | Count |
---|---|---|---|
GO:0006790 | sulfur compound metabolic process | 3 | 18 |
GO:0008152 | metabolic process | 1 | 18 |
GO:0009987 | cellular process | 1 | 18 |
GO:0016043 | cellular component organization | 3 | 18 |
GO:0016226 | iron-sulfur cluster assembly | 4 | 18 |
GO:0022607 | cellular component assembly | 4 | 18 |
GO:0031163 | metallo-sulfur cluster assembly | 5 | 18 |
GO:0044237 | cellular metabolic process | 2 | 18 |
GO:0071840 | cellular component organization or biogenesis | 2 | 18 |
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 | 18 |
GO:0005506 | iron ion binding | 6 | 18 |
GO:0043167 | ion binding | 2 | 18 |
GO:0043169 | cation binding | 3 | 18 |
GO:0046872 | metal ion binding | 4 | 18 |
GO:0046914 | transition metal ion binding | 5 | 18 |
GO:0051536 | iron-sulfur cluster binding | 3 | 18 |
GO:0051540 | metal cluster binding | 2 | 18 |
GO:0051539 | 4 iron, 4 sulfur cluster binding | 4 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 225 | 229 | PF00656 | 0.440 |
CLV_NRD_NRD_1 | 44 | 46 | PF00675 | 0.447 |
CLV_NRD_NRD_1 | 49 | 51 | PF00675 | 0.467 |
CLV_PCSK_KEX2_1 | 44 | 46 | PF00082 | 0.490 |
CLV_PCSK_KEX2_1 | 49 | 51 | PF00082 | 0.480 |
CLV_PCSK_PC7_1 | 45 | 51 | PF00082 | 0.578 |
CLV_PCSK_SKI1_1 | 17 | 21 | PF00082 | 0.469 |
CLV_PCSK_SKI1_1 | 178 | 182 | PF00082 | 0.270 |
CLV_PCSK_SKI1_1 | 232 | 236 | PF00082 | 0.256 |
CLV_PCSK_SKI1_1 | 264 | 268 | PF00082 | 0.598 |
CLV_Separin_Metazoa | 179 | 183 | PF03568 | 0.423 |
DOC_CKS1_1 | 57 | 62 | PF01111 | 0.284 |
DOC_CYCLIN_RxL_1 | 175 | 183 | PF00134 | 0.300 |
DOC_MAPK_MEF2A_6 | 204 | 212 | PF00069 | 0.440 |
DOC_PP1_RVXF_1 | 129 | 135 | PF00149 | 0.320 |
DOC_PP1_RVXF_1 | 15 | 21 | PF00149 | 0.384 |
DOC_PP1_RVXF_1 | 195 | 202 | PF00149 | 0.410 |
DOC_PP1_RVXF_1 | 87 | 94 | PF00149 | 0.284 |
DOC_PP4_FxxP_1 | 113 | 116 | PF00568 | 0.260 |
DOC_PP4_FxxP_1 | 67 | 70 | PF00568 | 0.260 |
DOC_USP7_MATH_1 | 21 | 25 | PF00917 | 0.461 |
DOC_USP7_MATH_1 | 70 | 74 | PF00917 | 0.304 |
DOC_USP7_UBL2_3 | 264 | 268 | PF12436 | 0.465 |
DOC_WW_Pin1_4 | 149 | 154 | PF00397 | 0.356 |
DOC_WW_Pin1_4 | 283 | 288 | PF00397 | 0.559 |
DOC_WW_Pin1_4 | 56 | 61 | PF00397 | 0.271 |
LIG_14-3-3_CanoR_1 | 2 | 7 | PF00244 | 0.527 |
LIG_14-3-3_CanoR_1 | 37 | 43 | PF00244 | 0.464 |
LIG_14-3-3_CanoR_1 | 44 | 48 | PF00244 | 0.469 |
LIG_deltaCOP1_diTrp_1 | 128 | 134 | PF00928 | 0.246 |
LIG_eIF4E_1 | 13 | 19 | PF01652 | 0.385 |
LIG_eIF4E_1 | 253 | 259 | PF01652 | 0.370 |
LIG_FHA_1 | 203 | 209 | PF00498 | 0.440 |
LIG_FHA_1 | 240 | 246 | PF00498 | 0.457 |
LIG_FHA_1 | 284 | 290 | PF00498 | 0.505 |
LIG_FHA_2 | 123 | 129 | PF00498 | 0.419 |
LIG_FHA_2 | 156 | 162 | PF00498 | 0.467 |
LIG_FHA_2 | 167 | 173 | PF00498 | 0.454 |
LIG_FHA_2 | 223 | 229 | PF00498 | 0.423 |
LIG_LIR_Apic_2 | 111 | 116 | PF02991 | 0.239 |
LIG_LIR_Apic_2 | 66 | 70 | PF02991 | 0.322 |
LIG_LIR_Gen_1 | 122 | 132 | PF02991 | 0.276 |
LIG_LIR_Gen_1 | 156 | 164 | PF02991 | 0.433 |
LIG_LIR_Gen_1 | 291 | 298 | PF02991 | 0.501 |
LIG_LIR_Gen_1 | 72 | 79 | PF02991 | 0.280 |
LIG_LIR_Nem_3 | 122 | 127 | PF02991 | 0.273 |
LIG_LIR_Nem_3 | 128 | 132 | PF02991 | 0.262 |
LIG_LIR_Nem_3 | 156 | 160 | PF02991 | 0.406 |
LIG_LIR_Nem_3 | 254 | 259 | PF02991 | 0.379 |
LIG_LIR_Nem_3 | 291 | 295 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 72 | 77 | PF02991 | 0.286 |
LIG_Pex14_1 | 34 | 38 | PF04695 | 0.355 |
LIG_SH2_CRK | 256 | 260 | PF00017 | 0.453 |
LIG_SH2_CRK | 292 | 296 | PF00017 | 0.565 |
LIG_SH2_GRB2like | 124 | 127 | PF00017 | 0.249 |
LIG_SH2_NCK_1 | 124 | 128 | PF00017 | 0.249 |
LIG_SH2_NCK_1 | 157 | 161 | PF00017 | 0.339 |
LIG_SH2_STAP1 | 105 | 109 | PF00017 | 0.144 |
LIG_SH2_STAT5 | 124 | 127 | PF00017 | 0.362 |
LIG_SH2_STAT5 | 143 | 146 | PF00017 | 0.237 |
LIG_SH2_STAT5 | 157 | 160 | PF00017 | 0.485 |
LIG_TYR_ITIM | 290 | 295 | PF00017 | 0.590 |
LIG_WRC_WIRS_1 | 136 | 141 | PF05994 | 0.231 |
LIG_WRC_WIRS_1 | 74 | 79 | PF05994 | 0.376 |
MOD_CDC14_SPxK_1 | 152 | 155 | PF00782 | 0.357 |
MOD_CDK_SPxK_1 | 149 | 155 | PF00069 | 0.364 |
MOD_CK1_1 | 122 | 128 | PF00069 | 0.324 |
MOD_CK1_1 | 135 | 141 | PF00069 | 0.173 |
MOD_CK1_1 | 222 | 228 | PF00069 | 0.425 |
MOD_CK1_1 | 23 | 29 | PF00069 | 0.664 |
MOD_CK1_1 | 7 | 13 | PF00069 | 0.635 |
MOD_CK1_1 | 73 | 79 | PF00069 | 0.404 |
MOD_CK2_1 | 122 | 128 | PF00069 | 0.346 |
MOD_CK2_1 | 155 | 161 | PF00069 | 0.425 |
MOD_CK2_1 | 166 | 172 | PF00069 | 0.381 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.460 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.433 |
MOD_GSK3_1 | 202 | 209 | PF00069 | 0.430 |
MOD_GSK3_1 | 215 | 222 | PF00069 | 0.445 |
MOD_N-GLC_1 | 146 | 151 | PF02516 | 0.363 |
MOD_N-GLC_1 | 7 | 12 | PF02516 | 0.384 |
MOD_N-GLC_2 | 148 | 150 | PF02516 | 0.406 |
MOD_NEK2_1 | 146 | 151 | PF00069 | 0.403 |
MOD_NEK2_1 | 20 | 25 | PF00069 | 0.635 |
MOD_NEK2_1 | 38 | 43 | PF00069 | 0.482 |
MOD_NEK2_1 | 6 | 11 | PF00069 | 0.478 |
MOD_NEK2_1 | 63 | 68 | PF00069 | 0.392 |
MOD_PIKK_1 | 103 | 109 | PF00454 | 0.144 |
MOD_PIKK_1 | 219 | 225 | PF00454 | 0.423 |
MOD_PIKK_1 | 24 | 30 | PF00454 | 0.380 |
MOD_PIKK_1 | 95 | 101 | PF00454 | 0.320 |
MOD_PK_1 | 117 | 123 | PF00069 | 0.260 |
MOD_PKA_2 | 43 | 49 | PF00069 | 0.437 |
MOD_Plk_1 | 132 | 138 | PF00069 | 0.242 |
MOD_Plk_1 | 146 | 152 | PF00069 | 0.386 |
MOD_Plk_1 | 155 | 161 | PF00069 | 0.472 |
MOD_Plk_4 | 108 | 114 | PF00069 | 0.296 |
MOD_Plk_4 | 135 | 141 | PF00069 | 0.236 |
MOD_Plk_4 | 155 | 161 | PF00069 | 0.264 |
MOD_Plk_4 | 285 | 291 | PF00069 | 0.513 |
MOD_Plk_4 | 38 | 44 | PF00069 | 0.542 |
MOD_Plk_4 | 73 | 79 | PF00069 | 0.332 |
MOD_ProDKin_1 | 149 | 155 | PF00069 | 0.364 |
MOD_ProDKin_1 | 283 | 289 | PF00069 | 0.558 |
MOD_ProDKin_1 | 56 | 62 | PF00069 | 0.271 |
MOD_SUMO_rev_2 | 161 | 169 | PF00179 | 0.504 |
MOD_SUMO_rev_2 | 192 | 199 | PF00179 | 0.431 |
TRG_DiLeu_BaEn_1 | 254 | 259 | PF01217 | 0.376 |
TRG_ENDOCYTIC_2 | 124 | 127 | PF00928 | 0.301 |
TRG_ENDOCYTIC_2 | 143 | 146 | PF00928 | 0.271 |
TRG_ENDOCYTIC_2 | 157 | 160 | PF00928 | 0.437 |
TRG_ENDOCYTIC_2 | 256 | 259 | PF00928 | 0.415 |
TRG_ENDOCYTIC_2 | 292 | 295 | PF00928 | 0.536 |
TRG_ER_diArg_1 | 43 | 45 | PF00400 | 0.495 |
TRG_ER_diArg_1 | 49 | 51 | PF00400 | 0.482 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I2Q0 | Leptomonas seymouri | 35% | 100% |
A0A0N1I735 | Leptomonas seymouri | 83% | 100% |
A0A0S4IJH0 | Bodo saltans | 35% | 100% |
A0A0S4IVB5 | Bodo saltans | 59% | 100% |
A0A1X0NST9 | Trypanosomatidae | 33% | 100% |
A0A1X0P8F8 | Trypanosomatidae | 69% | 100% |
A0A3S5H7F5 | Leishmania donovani | 32% | 100% |
A0A3S7XAI2 | Leishmania donovani | 95% | 100% |
A4HEM5 | Leishmania braziliensis | 35% | 100% |
A4HNU8 | Leishmania braziliensis | 94% | 100% |
A4I1V6 | Leishmania infantum | 32% | 100% |
A4ICP6 | Leishmania infantum | 95% | 100% |
B3MRT7 | Drosophila ananassae | 29% | 100% |
B3NYF7 | Drosophila erecta | 30% | 100% |
B4H303 | Drosophila persimilis | 29% | 100% |
B4IMF6 | Drosophila sechellia | 29% | 100% |
B4JWR9 | Drosophila grimshawi | 29% | 100% |
B4M375 | Drosophila virilis | 29% | 100% |
B4NE93 | Drosophila willistoni | 30% | 100% |
B4PZ52 | Drosophila yakuba | 30% | 100% |
B4R3T1 | Drosophila simulans | 31% | 100% |
B5DKJ8 | Drosophila pseudoobscura pseudoobscura | 29% | 100% |
C9ZS65 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
D0A2R6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 69% | 100% |
E9AY01 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
P32860 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 29% | 100% |
Q4Q1Y8 | Leishmania major | 91% | 100% |
Q4Q9H2 | Leishmania major | 33% | 100% |
Q8SY96 | Drosophila melanogaster | 29% | 100% |
Q9C8J2 | Arabidopsis thaliana | 33% | 100% |
Q9LIG6 | Arabidopsis thaliana | 32% | 100% |
Q9QZ23 | Mus musculus | 32% | 100% |
Q9UUB8 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 33% | 100% |
V5DRN0 | Trypanosoma cruzi | 73% | 100% |