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:0005759 | mitochondrial matrix | 5 | 2 |
GO:0005829 | cytosol | 2 | 2 |
GO:0031974 | membrane-enclosed lumen | 2 | 2 |
GO:0043233 | organelle lumen | 3 | 2 |
GO:0070013 | intracellular organelle lumen | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:0005739 | mitochondrion | 5 | 10 |
GO:0043226 | organelle | 2 | 10 |
GO:0043227 | membrane-bounded organelle | 3 | 10 |
GO:0043229 | intracellular organelle | 3 | 10 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 10 |
Related structures:
AlphaFold database: Q4QAF7
Term | Name | Level | Count |
---|---|---|---|
GO:0006790 | sulfur compound metabolic process | 3 | 2 |
GO:0008152 | metabolic process | 1 | 3 |
GO:0009987 | cellular process | 1 | 2 |
GO:0016043 | cellular component organization | 3 | 2 |
GO:0016226 | iron-sulfur cluster assembly | 4 | 2 |
GO:0022607 | cellular component assembly | 4 | 2 |
GO:0031163 | metallo-sulfur cluster assembly | 5 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
GO:0032259 | methylation | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 2 |
GO:0005542 | folic acid binding | 3 | 2 |
GO:0019842 | vitamin binding | 3 | 2 |
GO:0031406 | carboxylic acid binding | 4 | 2 |
GO:0033218 | amide binding | 2 | 2 |
GO:0036094 | small molecule binding | 2 | 2 |
GO:0043167 | ion binding | 2 | 2 |
GO:0043168 | anion binding | 3 | 2 |
GO:0043177 | organic acid binding | 3 | 2 |
GO:0072341 | modified amino acid binding | 2 | 2 |
GO:0097159 | organic cyclic compound binding | 2 | 2 |
GO:1901363 | heterocyclic compound binding | 2 | 2 |
GO:0003824 | catalytic activity | 1 | 3 |
GO:0008168 | methyltransferase activity | 4 | 1 |
GO:0016740 | transferase activity | 2 | 3 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 2 |
GO:0004047 | aminomethyltransferase activity | 5 | 1 |
GO:0016742 | hydroxymethyl-, formyl- and related transferase activity | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 118 | 122 | PF00656 | 0.609 |
CLV_C14_Caspase3-7 | 200 | 204 | PF00656 | 0.347 |
CLV_NRD_NRD_1 | 14 | 16 | PF00675 | 0.461 |
CLV_NRD_NRD_1 | 186 | 188 | PF00675 | 0.490 |
CLV_NRD_NRD_1 | 261 | 263 | PF00675 | 0.414 |
CLV_NRD_NRD_1 | 356 | 358 | PF00675 | 0.521 |
CLV_NRD_NRD_1 | 96 | 98 | PF00675 | 0.255 |
CLV_PCSK_KEX2_1 | 14 | 16 | PF00082 | 0.461 |
CLV_PCSK_KEX2_1 | 263 | 265 | PF00082 | 0.371 |
CLV_PCSK_PC1ET2_1 | 263 | 265 | PF00082 | 0.371 |
CLV_PCSK_PC7_1 | 10 | 16 | PF00082 | 0.476 |
CLV_PCSK_SKI1_1 | 14 | 18 | PF00082 | 0.430 |
CLV_PCSK_SKI1_1 | 358 | 362 | PF00082 | 0.472 |
CLV_PCSK_SKI1_1 | 82 | 86 | PF00082 | 0.297 |
DEG_SPOP_SBC_1 | 169 | 173 | PF00917 | 0.599 |
DOC_ANK_TNKS_1 | 211 | 218 | PF00023 | 0.482 |
DOC_CYCLIN_RxL_1 | 222 | 230 | PF00134 | 0.390 |
DOC_MAPK_DCC_7 | 331 | 341 | PF00069 | 0.539 |
DOC_MAPK_gen_1 | 262 | 270 | PF00069 | 0.380 |
DOC_MAPK_gen_1 | 95 | 102 | PF00069 | 0.455 |
DOC_MAPK_MEF2A_6 | 262 | 270 | PF00069 | 0.395 |
DOC_PP1_RVXF_1 | 235 | 242 | PF00149 | 0.378 |
DOC_PP4_FxxP_1 | 155 | 158 | PF00568 | 0.412 |
DOC_PP4_FxxP_1 | 164 | 167 | PF00568 | 0.595 |
DOC_USP7_MATH_1 | 122 | 126 | PF00917 | 0.665 |
DOC_USP7_MATH_1 | 134 | 138 | PF00917 | 0.740 |
DOC_USP7_MATH_1 | 170 | 174 | PF00917 | 0.699 |
DOC_USP7_MATH_1 | 41 | 45 | PF00917 | 0.454 |
DOC_USP7_UBL2_3 | 358 | 362 | PF12436 | 0.473 |
DOC_USP7_UBL2_3 | 95 | 99 | PF12436 | 0.515 |
DOC_WW_Pin1_4 | 140 | 145 | PF00397 | 0.624 |
DOC_WW_Pin1_4 | 171 | 176 | PF00397 | 0.630 |
DOC_WW_Pin1_4 | 178 | 183 | PF00397 | 0.513 |
DOC_WW_Pin1_4 | 198 | 203 | PF00397 | 0.568 |
DOC_WW_Pin1_4 | 342 | 347 | PF00397 | 0.578 |
LIG_14-3-3_CanoR_1 | 150 | 158 | PF00244 | 0.542 |
LIG_14-3-3_CanoR_1 | 262 | 267 | PF00244 | 0.385 |
LIG_14-3-3_CanoR_1 | 82 | 91 | PF00244 | 0.491 |
LIG_Actin_WH2_2 | 312 | 329 | PF00022 | 0.412 |
LIG_APCC_ABBAyCdc20_2 | 97 | 103 | PF00400 | 0.531 |
LIG_BRCT_BRCA1_1 | 180 | 184 | PF00533 | 0.383 |
LIG_BRCT_BRCA1_1 | 225 | 229 | PF00533 | 0.420 |
LIG_EVH1_1 | 164 | 168 | PF00568 | 0.422 |
LIG_FHA_1 | 204 | 210 | PF00498 | 0.517 |
LIG_FHA_1 | 263 | 269 | PF00498 | 0.386 |
LIG_FHA_1 | 290 | 296 | PF00498 | 0.596 |
LIG_FHA_1 | 31 | 37 | PF00498 | 0.474 |
LIG_FHA_1 | 331 | 337 | PF00498 | 0.577 |
LIG_FHA_1 | 51 | 57 | PF00498 | 0.465 |
LIG_FHA_1 | 83 | 89 | PF00498 | 0.392 |
LIG_FHA_2 | 116 | 122 | PF00498 | 0.559 |
LIG_FHA_2 | 144 | 150 | PF00498 | 0.617 |
LIG_LIR_Apic_2 | 152 | 158 | PF02991 | 0.423 |
LIG_LIR_Apic_2 | 161 | 167 | PF02991 | 0.467 |
LIG_LIR_Apic_2 | 194 | 198 | PF02991 | 0.555 |
LIG_LIR_Gen_1 | 203 | 210 | PF02991 | 0.440 |
LIG_LIR_LC3C_4 | 108 | 111 | PF02991 | 0.516 |
LIG_LIR_Nem_3 | 203 | 208 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 44 | 49 | PF02991 | 0.451 |
LIG_SH2_CRK | 205 | 209 | PF00017 | 0.504 |
LIG_SH2_STAP1 | 205 | 209 | PF00017 | 0.417 |
LIG_SH2_STAT3 | 246 | 249 | PF00017 | 0.359 |
LIG_SH2_STAT5 | 205 | 208 | PF00017 | 0.450 |
LIG_SH2_STAT5 | 246 | 249 | PF00017 | 0.374 |
LIG_SH2_STAT5 | 328 | 331 | PF00017 | 0.423 |
LIG_SH2_STAT5 | 51 | 54 | PF00017 | 0.515 |
LIG_SH3_3 | 162 | 168 | PF00018 | 0.599 |
LIG_SH3_3 | 176 | 182 | PF00018 | 0.663 |
LIG_SH3_3 | 272 | 278 | PF00018 | 0.594 |
LIG_SH3_3 | 294 | 300 | PF00018 | 0.527 |
LIG_SUMO_SIM_anti_2 | 108 | 113 | PF11976 | 0.481 |
LIG_SUMO_SIM_anti_2 | 255 | 261 | PF11976 | 0.424 |
LIG_SUMO_SIM_par_1 | 292 | 299 | PF11976 | 0.559 |
LIG_SUMO_SIM_par_1 | 74 | 81 | PF11976 | 0.496 |
LIG_TRAF2_1 | 114 | 117 | PF00917 | 0.552 |
LIG_TRAF2_1 | 146 | 149 | PF00917 | 0.669 |
LIG_UBA3_1 | 323 | 331 | PF00899 | 0.495 |
LIG_UBA3_1 | 87 | 95 | PF00899 | 0.485 |
MOD_CK1_1 | 125 | 131 | PF00069 | 0.725 |
MOD_CK1_1 | 137 | 143 | PF00069 | 0.673 |
MOD_CK1_1 | 171 | 177 | PF00069 | 0.686 |
MOD_CK1_1 | 201 | 207 | PF00069 | 0.465 |
MOD_CK2_1 | 143 | 149 | PF00069 | 0.649 |
MOD_CK2_1 | 80 | 86 | PF00069 | 0.524 |
MOD_GlcNHglycan | 116 | 121 | PF01048 | 0.552 |
MOD_GlcNHglycan | 127 | 130 | PF01048 | 0.723 |
MOD_GlcNHglycan | 302 | 305 | PF01048 | 0.497 |
MOD_GlcNHglycan | 81 | 85 | PF01048 | 0.335 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.717 |
MOD_GSK3_1 | 197 | 204 | PF00069 | 0.584 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.412 |
MOD_GSK3_1 | 342 | 349 | PF00069 | 0.516 |
MOD_LATS_1 | 80 | 86 | PF00433 | 0.392 |
MOD_N-GLC_1 | 223 | 228 | PF02516 | 0.524 |
MOD_NEK2_1 | 115 | 120 | PF00069 | 0.504 |
MOD_NEK2_1 | 208 | 213 | PF00069 | 0.403 |
MOD_NEK2_1 | 258 | 263 | PF00069 | 0.443 |
MOD_NEK2_1 | 50 | 55 | PF00069 | 0.454 |
MOD_NEK2_2 | 41 | 46 | PF00069 | 0.515 |
MOD_PK_1 | 135 | 141 | PF00069 | 0.741 |
MOD_PKA_1 | 262 | 268 | PF00069 | 0.379 |
MOD_PKA_2 | 125 | 131 | PF00069 | 0.678 |
MOD_PKA_2 | 134 | 140 | PF00069 | 0.647 |
MOD_PKA_2 | 149 | 155 | PF00069 | 0.569 |
MOD_PKA_2 | 19 | 25 | PF00069 | 0.508 |
MOD_Plk_1 | 135 | 141 | PF00069 | 0.744 |
MOD_Plk_1 | 223 | 229 | PF00069 | 0.494 |
MOD_Plk_4 | 204 | 210 | PF00069 | 0.472 |
MOD_Plk_4 | 41 | 47 | PF00069 | 0.446 |
MOD_Plk_4 | 71 | 77 | PF00069 | 0.470 |
MOD_ProDKin_1 | 140 | 146 | PF00069 | 0.613 |
MOD_ProDKin_1 | 171 | 177 | PF00069 | 0.630 |
MOD_ProDKin_1 | 178 | 184 | PF00069 | 0.494 |
MOD_ProDKin_1 | 198 | 204 | PF00069 | 0.564 |
MOD_ProDKin_1 | 342 | 348 | PF00069 | 0.576 |
MOD_SUMO_rev_2 | 353 | 363 | PF00179 | 0.443 |
MOD_SUMO_rev_2 | 89 | 96 | PF00179 | 0.540 |
TRG_ENDOCYTIC_2 | 205 | 208 | PF00928 | 0.372 |
TRG_ENDOCYTIC_2 | 46 | 49 | PF00928 | 0.515 |
TRG_ER_diArg_1 | 14 | 16 | PF00400 | 0.461 |
TRG_ER_diArg_1 | 17 | 20 | PF00400 | 0.540 |
TRG_ER_diArg_1 | 324 | 327 | PF00400 | 0.386 |
TRG_NLS_MonoExtN_4 | 95 | 101 | PF00514 | 0.479 |
TRG_Pf-PMV_PEXEL_1 | 212 | 216 | PF00026 | 0.480 |
TRG_Pf-PMV_PEXEL_1 | 55 | 59 | PF00026 | 0.340 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IM11 | Leptomonas seymouri | 60% | 84% |
A0A0S4JL83 | Bodo saltans | 39% | 100% |
A0A1X0NVS6 | Trypanosomatidae | 44% | 100% |
A0A3Q8IEZ2 | Leishmania donovani | 86% | 94% |
A0A3R7K245 | Trypanosoma rangeli | 50% | 100% |
A2R472 | Aspergillus niger (strain CBS 513.88 / FGSC A1513) | 29% | 83% |
A4HDN4 | Leishmania braziliensis | 78% | 93% |
A4R8F9 | Magnaporthe oryzae (strain 70-15 / ATCC MYA-4617 / FGSC 8958) | 29% | 95% |
B8JMH0 | Danio rerio | 30% | 100% |
C9ZWC9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 46% | 100% |
E9AH81 | Leishmania infantum | 86% | 94% |
E9AX19 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 95% |
P0CM52 | Cryptococcus neoformans var. neoformans serotype D (strain JEC21 / ATCC MYA-565) | 28% | 98% |
P0CM53 | Cryptococcus neoformans var. neoformans serotype D (strain B-3501A) | 28% | 98% |
Q09929 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 27% | 100% |
Q0UE25 | Phaeosphaeria nodorum (strain SN15 / ATCC MYA-4574 / FGSC 10173) | 24% | 91% |
Q1DK38 | Coccidioides immitis (strain RS) | 27% | 87% |
Q2H6N9 | Chaetomium globosum (strain ATCC 6205 / CBS 148.51 / DSM 1962 / NBRC 6347 / NRRL 1970) | 30% | 84% |
Q2U664 | Aspergillus oryzae (strain ATCC 42149 / RIB 40) | 30% | 82% |
Q4P7A4 | Ustilago maydis (strain 521 / FGSC 9021) | 29% | 91% |
Q54NS1 | Dictyostelium discoideum | 28% | 90% |
Q5T440 | Homo sapiens | 30% | 100% |
Q6C8Y7 | Yarrowia lipolytica (strain CLIB 122 / E 150) | 30% | 77% |
Q6FSH5 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 22% | 74% |
Q7RYZ1 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 31% | 84% |
Q8CAK1 | Mus musculus | 32% | 100% |
Q8L733 | Arabidopsis thaliana | 26% | 94% |
V5AJ90 | Trypanosoma cruzi | 49% | 100% |