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: 14 |
NetGPI | no | yes: 0, no: 14 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 2 |
GO:0005739 | mitochondrion | 5 | 3 |
GO:0043226 | organelle | 2 | 3 |
GO:0043227 | membrane-bounded organelle | 3 | 3 |
GO:0043229 | intracellular organelle | 3 | 3 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 3 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
Related structures:
AlphaFold database: Q4Q1Y8
Term | Name | Level | Count |
---|---|---|---|
GO:0006790 | sulfur compound metabolic process | 3 | 15 |
GO:0006807 | nitrogen compound metabolic process | 2 | 3 |
GO:0008152 | metabolic process | 1 | 15 |
GO:0009987 | cellular process | 1 | 15 |
GO:0016043 | cellular component organization | 3 | 15 |
GO:0016226 | iron-sulfur cluster assembly | 4 | 15 |
GO:0019538 | protein metabolic process | 3 | 3 |
GO:0022607 | cellular component assembly | 4 | 15 |
GO:0031163 | metallo-sulfur cluster assembly | 5 | 15 |
GO:0043170 | macromolecule metabolic process | 3 | 3 |
GO:0044237 | cellular metabolic process | 2 | 15 |
GO:0044238 | primary metabolic process | 2 | 3 |
GO:0051604 | protein maturation | 4 | 3 |
GO:0071704 | organic substance metabolic process | 2 | 3 |
GO:0071840 | cellular component organization or biogenesis | 2 | 15 |
GO:0097428 | protein maturation by iron-sulfur cluster transfer | 5 | 3 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 3 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 15 |
GO:0005506 | iron ion binding | 6 | 15 |
GO:0043167 | ion binding | 2 | 15 |
GO:0043169 | cation binding | 3 | 15 |
GO:0046872 | metal ion binding | 4 | 15 |
GO:0046914 | transition metal ion binding | 5 | 15 |
GO:0051536 | iron-sulfur cluster binding | 3 | 15 |
GO:0051539 | 4 iron, 4 sulfur cluster binding | 4 | 3 |
GO:0051540 | metal cluster binding | 2 | 15 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 235 | 239 | PF00656 | 0.438 |
CLV_NRD_NRD_1 | 54 | 56 | PF00675 | 0.435 |
CLV_PCSK_KEX2_1 | 54 | 56 | PF00082 | 0.475 |
CLV_PCSK_SKI1_1 | 188 | 192 | PF00082 | 0.259 |
CLV_PCSK_SKI1_1 | 242 | 246 | PF00082 | 0.220 |
CLV_PCSK_SKI1_1 | 27 | 31 | PF00082 | 0.433 |
CLV_PCSK_SKI1_1 | 274 | 278 | PF00082 | 0.615 |
CLV_PCSK_SKI1_1 | 287 | 291 | PF00082 | 0.427 |
CLV_Separin_Metazoa | 189 | 193 | PF03568 | 0.420 |
DEG_APCC_DBOX_1 | 291 | 299 | PF00400 | 0.612 |
DOC_CKS1_1 | 67 | 72 | PF01111 | 0.281 |
DOC_CYCLIN_RxL_1 | 185 | 193 | PF00134 | 0.311 |
DOC_MAPK_MEF2A_6 | 214 | 222 | PF00069 | 0.439 |
DOC_PP1_RVXF_1 | 139 | 145 | PF00149 | 0.316 |
DOC_PP1_RVXF_1 | 205 | 212 | PF00149 | 0.408 |
DOC_PP1_RVXF_1 | 97 | 104 | PF00149 | 0.281 |
DOC_PP2B_LxvP_1 | 17 | 20 | PF13499 | 0.484 |
DOC_PP4_FxxP_1 | 123 | 126 | PF00568 | 0.257 |
DOC_PP4_FxxP_1 | 77 | 80 | PF00568 | 0.260 |
DOC_USP7_MATH_1 | 31 | 35 | PF00917 | 0.687 |
DOC_USP7_MATH_1 | 80 | 84 | PF00917 | 0.328 |
DOC_USP7_MATH_2 | 116 | 122 | PF00917 | 0.278 |
DOC_USP7_UBL2_3 | 274 | 278 | PF12436 | 0.475 |
DOC_WW_Pin1_4 | 15 | 20 | PF00397 | 0.559 |
DOC_WW_Pin1_4 | 159 | 164 | PF00397 | 0.358 |
DOC_WW_Pin1_4 | 21 | 26 | PF00397 | 0.542 |
DOC_WW_Pin1_4 | 293 | 298 | PF00397 | 0.570 |
DOC_WW_Pin1_4 | 66 | 71 | PF00397 | 0.284 |
LIG_14-3-3_CanoR_1 | 3 | 8 | PF00244 | 0.439 |
LIG_14-3-3_CanoR_1 | 47 | 53 | PF00244 | 0.456 |
LIG_14-3-3_CanoR_1 | 54 | 58 | PF00244 | 0.452 |
LIG_Actin_WH2_2 | 38 | 56 | PF00022 | 0.346 |
LIG_deltaCOP1_diTrp_1 | 138 | 144 | PF00928 | 0.258 |
LIG_eIF4E_1 | 263 | 269 | PF01652 | 0.349 |
LIG_FHA_1 | 179 | 185 | PF00498 | 0.418 |
LIG_FHA_1 | 213 | 219 | PF00498 | 0.448 |
LIG_FHA_1 | 250 | 256 | PF00498 | 0.438 |
LIG_FHA_1 | 294 | 300 | PF00498 | 0.475 |
LIG_FHA_1 | 4 | 10 | PF00498 | 0.435 |
LIG_FHA_1 | 44 | 50 | PF00498 | 0.590 |
LIG_FHA_1 | 74 | 80 | PF00498 | 0.203 |
LIG_FHA_2 | 133 | 139 | PF00498 | 0.418 |
LIG_FHA_2 | 166 | 172 | PF00498 | 0.442 |
LIG_FHA_2 | 177 | 183 | PF00498 | 0.443 |
LIG_FHA_2 | 233 | 239 | PF00498 | 0.420 |
LIG_LIR_Apic_2 | 121 | 126 | PF02991 | 0.236 |
LIG_LIR_Apic_2 | 76 | 80 | PF02991 | 0.336 |
LIG_LIR_Gen_1 | 132 | 142 | PF02991 | 0.282 |
LIG_LIR_Gen_1 | 166 | 174 | PF02991 | 0.382 |
LIG_LIR_Gen_1 | 301 | 308 | PF02991 | 0.490 |
LIG_LIR_Gen_1 | 82 | 89 | PF02991 | 0.276 |
LIG_LIR_Nem_3 | 132 | 137 | PF02991 | 0.276 |
LIG_LIR_Nem_3 | 138 | 142 | PF02991 | 0.276 |
LIG_LIR_Nem_3 | 264 | 269 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 301 | 305 | PF02991 | 0.524 |
LIG_LIR_Nem_3 | 82 | 87 | PF02991 | 0.258 |
LIG_Pex14_1 | 44 | 48 | PF04695 | 0.363 |
LIG_SH2_CRK | 266 | 270 | PF00017 | 0.418 |
LIG_SH2_GRB2like | 134 | 137 | PF00017 | 0.262 |
LIG_SH2_NCK_1 | 134 | 138 | PF00017 | 0.262 |
LIG_SH2_STAT5 | 134 | 137 | PF00017 | 0.379 |
LIG_SH2_STAT5 | 153 | 156 | PF00017 | 0.212 |
LIG_SH2_STAT5 | 167 | 170 | PF00017 | 0.331 |
LIG_SH2_STAT5 | 7 | 10 | PF00017 | 0.440 |
LIG_SH3_2 | 22 | 27 | PF14604 | 0.385 |
LIG_SH3_3 | 16 | 22 | PF00018 | 0.561 |
LIG_TYR_ITIM | 300 | 305 | PF00017 | 0.583 |
LIG_WRC_WIRS_1 | 146 | 151 | PF05994 | 0.239 |
LIG_WRC_WIRS_1 | 84 | 89 | PF05994 | 0.373 |
MOD_CDC14_SPxK_1 | 162 | 165 | PF00782 | 0.366 |
MOD_CDC14_SPxK_1 | 24 | 27 | PF00782 | 0.392 |
MOD_CDK_SPxK_1 | 159 | 165 | PF00069 | 0.367 |
MOD_CDK_SPxK_1 | 21 | 27 | PF00069 | 0.383 |
MOD_CK1_1 | 132 | 138 | PF00069 | 0.328 |
MOD_CK1_1 | 145 | 151 | PF00069 | 0.178 |
MOD_CK1_1 | 23 | 29 | PF00069 | 0.637 |
MOD_CK1_1 | 232 | 238 | PF00069 | 0.446 |
MOD_CK1_1 | 33 | 39 | PF00069 | 0.619 |
MOD_CK1_1 | 43 | 49 | PF00069 | 0.589 |
MOD_CK1_1 | 83 | 89 | PF00069 | 0.290 |
MOD_CK2_1 | 137 | 143 | PF00069 | 0.339 |
MOD_CK2_1 | 165 | 171 | PF00069 | 0.410 |
MOD_CK2_1 | 176 | 182 | PF00069 | 0.378 |
MOD_GSK3_1 | 212 | 219 | PF00069 | 0.408 |
MOD_GSK3_1 | 225 | 232 | PF00069 | 0.434 |
MOD_GSK3_1 | 29 | 36 | PF00069 | 0.647 |
MOD_GSK3_1 | 43 | 50 | PF00069 | 0.646 |
MOD_N-GLC_1 | 293 | 298 | PF02516 | 0.387 |
MOD_N-GLC_2 | 158 | 160 | PF02516 | 0.368 |
MOD_NEK2_1 | 154 | 159 | PF00069 | 0.406 |
MOD_NEK2_1 | 30 | 35 | PF00069 | 0.582 |
MOD_NEK2_1 | 48 | 53 | PF00069 | 0.464 |
MOD_NEK2_1 | 73 | 78 | PF00069 | 0.429 |
MOD_PIKK_1 | 105 | 111 | PF00454 | 0.316 |
MOD_PIKK_1 | 229 | 235 | PF00454 | 0.420 |
MOD_PK_1 | 127 | 133 | PF00069 | 0.260 |
MOD_PKA_2 | 53 | 59 | PF00069 | 0.423 |
MOD_Plk_1 | 142 | 148 | PF00069 | 0.262 |
MOD_Plk_1 | 165 | 171 | PF00069 | 0.450 |
MOD_Plk_4 | 118 | 124 | PF00069 | 0.241 |
MOD_Plk_4 | 145 | 151 | PF00069 | 0.257 |
MOD_Plk_4 | 165 | 171 | PF00069 | 0.284 |
MOD_Plk_4 | 3 | 9 | PF00069 | 0.441 |
MOD_Plk_4 | 48 | 54 | PF00069 | 0.559 |
MOD_Plk_4 | 83 | 89 | PF00069 | 0.354 |
MOD_ProDKin_1 | 15 | 21 | PF00069 | 0.558 |
MOD_ProDKin_1 | 159 | 165 | PF00069 | 0.367 |
MOD_ProDKin_1 | 293 | 299 | PF00069 | 0.570 |
MOD_ProDKin_1 | 66 | 72 | PF00069 | 0.284 |
MOD_SUMO_rev_2 | 171 | 179 | PF00179 | 0.368 |
MOD_SUMO_rev_2 | 202 | 209 | PF00179 | 0.408 |
TRG_DiLeu_BaEn_1 | 264 | 269 | PF01217 | 0.355 |
TRG_ENDOCYTIC_2 | 134 | 137 | PF00928 | 0.309 |
TRG_ENDOCYTIC_2 | 153 | 156 | PF00928 | 0.225 |
TRG_ENDOCYTIC_2 | 167 | 170 | PF00928 | 0.307 |
TRG_ENDOCYTIC_2 | 266 | 269 | PF00928 | 0.343 |
TRG_ENDOCYTIC_2 | 302 | 305 | PF00928 | 0.530 |
TRG_ER_diArg_1 | 53 | 55 | PF00400 | 0.475 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I2Q0 | Leptomonas seymouri | 34% | 100% |
A0A0N1I735 | Leptomonas seymouri | 81% | 100% |
A0A0S4IVB5 | Bodo saltans | 58% | 100% |
A0A1X0P8F8 | Trypanosomatidae | 68% | 100% |
A0A3S5H7F5 | Leishmania donovani | 33% | 100% |
A0A3S7XAI2 | Leishmania donovani | 95% | 100% |
A4HEM5 | Leishmania braziliensis | 34% | 100% |
A4HNU8 | Leishmania braziliensis | 89% | 100% |
A4I1V6 | Leishmania infantum | 33% | 100% |
A4ICP6 | Leishmania infantum | 95% | 100% |
B3MRT7 | Drosophila ananassae | 26% | 100% |
B3NYF7 | Drosophila erecta | 27% | 100% |
B4H303 | Drosophila persimilis | 28% | 100% |
B4IMF6 | Drosophila sechellia | 27% | 100% |
B4JWR9 | Drosophila grimshawi | 27% | 100% |
B4M375 | Drosophila virilis | 28% | 100% |
B4NE93 | Drosophila willistoni | 28% | 100% |
B4PZ52 | Drosophila yakuba | 29% | 100% |
B4R3T1 | Drosophila simulans | 28% | 100% |
B5DKJ8 | Drosophila pseudoobscura pseudoobscura | 28% | 100% |
D0A2R6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 70% | 100% |
E9ASK8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
E9AY01 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 100% |
P32860 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 30% | 100% |
Q4Q9H2 | Leishmania major | 35% | 100% |
Q8SY96 | Drosophila melanogaster | 27% | 100% |
Q9C8J2 | Arabidopsis thaliana | 31% | 100% |
Q9QZ23 | Mus musculus | 33% | 100% |
V5DRN0 | Trypanosoma cruzi | 72% | 100% |