Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 2 |
Forrest at al. (procyclic) | no | yes: 2 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 3 |
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: 36 |
NetGPI | no | yes: 0, no: 36 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
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 |
Related structures:
AlphaFold database: A0A3S7WUK0
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 35 |
GO:0016787 | hydrolase activity | 2 | 35 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 403 | 405 | PF00675 | 0.459 |
CLV_PCSK_KEX2_1 | 276 | 278 | PF00082 | 0.264 |
CLV_PCSK_PC1ET2_1 | 276 | 278 | PF00082 | 0.313 |
CLV_PCSK_SKI1_1 | 269 | 273 | PF00082 | 0.305 |
CLV_PCSK_SKI1_1 | 286 | 290 | PF00082 | 0.179 |
CLV_PCSK_SKI1_1 | 324 | 328 | PF00082 | 0.195 |
DEG_APCC_DBOX_1 | 285 | 293 | PF00400 | 0.406 |
DEG_COP1_1 | 331 | 339 | PF00400 | 0.387 |
DEG_SPOP_SBC_1 | 207 | 211 | PF00917 | 0.412 |
DOC_CKS1_1 | 330 | 335 | PF01111 | 0.344 |
DOC_CYCLIN_RxL_1 | 172 | 183 | PF00134 | 0.278 |
DOC_MAPK_gen_1 | 273 | 281 | PF00069 | 0.404 |
DOC_MAPK_MEF2A_6 | 49 | 57 | PF00069 | 0.292 |
DOC_MIT_MIM_1 | 146 | 155 | PF04212 | 0.195 |
DOC_PP1_RVXF_1 | 147 | 153 | PF00149 | 0.195 |
DOC_PP2B_LxvP_1 | 10 | 13 | PF13499 | 0.678 |
DOC_PP2B_LxvP_1 | 292 | 295 | PF13499 | 0.362 |
DOC_PP2B_PxIxI_1 | 336 | 342 | PF00149 | 0.215 |
DOC_PP4_FxxP_1 | 334 | 337 | PF00568 | 0.195 |
DOC_USP7_MATH_1 | 398 | 402 | PF00917 | 0.431 |
DOC_USP7_MATH_1 | 5 | 9 | PF00917 | 0.734 |
DOC_USP7_UBL2_3 | 248 | 252 | PF12436 | 0.384 |
DOC_USP7_UBL2_3 | 422 | 426 | PF12436 | 0.690 |
DOC_WW_Pin1_4 | 185 | 190 | PF00397 | 0.320 |
DOC_WW_Pin1_4 | 329 | 334 | PF00397 | 0.257 |
DOC_WW_Pin1_4 | 58 | 63 | PF00397 | 0.294 |
DOC_WW_Pin1_4 | 8 | 13 | PF00397 | 0.578 |
LIG_14-3-3_CanoR_1 | 175 | 180 | PF00244 | 0.298 |
LIG_14-3-3_CanoR_1 | 238 | 246 | PF00244 | 0.295 |
LIG_14-3-3_CanoR_1 | 30 | 38 | PF00244 | 0.453 |
LIG_14-3-3_CanoR_1 | 302 | 311 | PF00244 | 0.340 |
LIG_14-3-3_CanoR_1 | 324 | 334 | PF00244 | 0.471 |
LIG_14-3-3_CanoR_1 | 355 | 361 | PF00244 | 0.334 |
LIG_14-3-3_CanoR_1 | 69 | 74 | PF00244 | 0.417 |
LIG_Actin_WH2_1 | 365 | 383 | PF00022 | 0.396 |
LIG_BIR_III_4 | 140 | 144 | PF00653 | 0.408 |
LIG_FHA_1 | 123 | 129 | PF00498 | 0.386 |
LIG_FHA_1 | 245 | 251 | PF00498 | 0.339 |
LIG_FHA_1 | 325 | 331 | PF00498 | 0.298 |
LIG_FHA_1 | 336 | 342 | PF00498 | 0.251 |
LIG_FHA_1 | 35 | 41 | PF00498 | 0.379 |
LIG_FHA_2 | 131 | 137 | PF00498 | 0.313 |
LIG_FHA_2 | 220 | 226 | PF00498 | 0.195 |
LIG_FHA_2 | 92 | 98 | PF00498 | 0.348 |
LIG_LIR_Apic_2 | 331 | 337 | PF02991 | 0.194 |
LIG_LIR_Gen_1 | 245 | 253 | PF02991 | 0.410 |
LIG_LIR_Gen_1 | 383 | 392 | PF02991 | 0.362 |
LIG_LIR_Gen_1 | 77 | 85 | PF02991 | 0.425 |
LIG_LIR_Nem_3 | 112 | 116 | PF02991 | 0.337 |
LIG_LIR_Nem_3 | 140 | 145 | PF02991 | 0.406 |
LIG_LIR_Nem_3 | 23 | 28 | PF02991 | 0.420 |
LIG_LIR_Nem_3 | 245 | 249 | PF02991 | 0.344 |
LIG_LIR_Nem_3 | 383 | 387 | PF02991 | 0.371 |
LIG_LIR_Nem_3 | 77 | 83 | PF02991 | 0.315 |
LIG_NRBOX | 69 | 75 | PF00104 | 0.268 |
LIG_PDZ_Class_1 | 426 | 431 | PF00595 | 0.695 |
LIG_SH2_CRK | 118 | 122 | PF00017 | 0.310 |
LIG_SH2_CRK | 80 | 84 | PF00017 | 0.475 |
LIG_SH2_PTP2 | 384 | 387 | PF00017 | 0.445 |
LIG_SH2_SRC | 116 | 119 | PF00017 | 0.215 |
LIG_SH2_STAP1 | 116 | 120 | PF00017 | 0.417 |
LIG_SH2_STAP1 | 214 | 218 | PF00017 | 0.410 |
LIG_SH2_STAP1 | 242 | 246 | PF00017 | 0.412 |
LIG_SH2_STAT5 | 113 | 116 | PF00017 | 0.412 |
LIG_SH2_STAT5 | 132 | 135 | PF00017 | 0.296 |
LIG_SH2_STAT5 | 335 | 338 | PF00017 | 0.391 |
LIG_SH2_STAT5 | 367 | 370 | PF00017 | 0.350 |
LIG_SH2_STAT5 | 384 | 387 | PF00017 | 0.403 |
LIG_SH3_3 | 1 | 7 | PF00018 | 0.708 |
LIG_SH3_3 | 104 | 110 | PF00018 | 0.442 |
LIG_SH3_3 | 15 | 21 | PF00018 | 0.575 |
LIG_SH3_3 | 327 | 333 | PF00018 | 0.329 |
LIG_SH3_3 | 344 | 350 | PF00018 | 0.289 |
LIG_SUMO_SIM_anti_2 | 178 | 184 | PF11976 | 0.237 |
LIG_SUMO_SIM_anti_2 | 201 | 207 | PF11976 | 0.428 |
LIG_SUMO_SIM_par_1 | 174 | 180 | PF11976 | 0.300 |
LIG_TRAF2_1 | 223 | 226 | PF00917 | 0.412 |
LIG_UBA3_1 | 199 | 208 | PF00899 | 0.368 |
LIG_WRC_WIRS_1 | 42 | 47 | PF05994 | 0.322 |
MOD_CDK_SPxxK_3 | 8 | 15 | PF00069 | 0.644 |
MOD_CK1_1 | 183 | 189 | PF00069 | 0.295 |
MOD_CK1_1 | 201 | 207 | PF00069 | 0.358 |
MOD_CK1_1 | 328 | 334 | PF00069 | 0.350 |
MOD_CK1_1 | 8 | 14 | PF00069 | 0.675 |
MOD_CK2_1 | 124 | 130 | PF00069 | 0.359 |
MOD_CK2_1 | 219 | 225 | PF00069 | 0.369 |
MOD_Cter_Amidation | 402 | 405 | PF01082 | 0.379 |
MOD_GlcNHglycan | 158 | 161 | PF01048 | 0.392 |
MOD_GlcNHglycan | 210 | 213 | PF01048 | 0.380 |
MOD_GlcNHglycan | 222 | 225 | PF01048 | 0.405 |
MOD_GlcNHglycan | 253 | 256 | PF01048 | 0.366 |
MOD_GlcNHglycan | 327 | 330 | PF01048 | 0.415 |
MOD_GlcNHglycan | 418 | 421 | PF01048 | 0.681 |
MOD_GlcNHglycan | 76 | 79 | PF01048 | 0.457 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.276 |
MOD_GSK3_1 | 275 | 282 | PF00069 | 0.237 |
MOD_GSK3_1 | 30 | 37 | PF00069 | 0.512 |
MOD_GSK3_1 | 320 | 327 | PF00069 | 0.425 |
MOD_N-GLC_1 | 320 | 325 | PF02516 | 0.215 |
MOD_NEK2_1 | 155 | 160 | PF00069 | 0.356 |
MOD_NEK2_1 | 177 | 182 | PF00069 | 0.297 |
MOD_NEK2_1 | 275 | 280 | PF00069 | 0.303 |
MOD_NEK2_1 | 311 | 316 | PF00069 | 0.229 |
MOD_NEK2_1 | 372 | 377 | PF00069 | 0.371 |
MOD_NEK2_1 | 380 | 385 | PF00069 | 0.390 |
MOD_NEK2_1 | 74 | 79 | PF00069 | 0.383 |
MOD_NEK2_2 | 124 | 129 | PF00069 | 0.463 |
MOD_PIKK_1 | 309 | 315 | PF00454 | 0.452 |
MOD_PK_1 | 304 | 310 | PF00069 | 0.417 |
MOD_PKA_2 | 219 | 225 | PF00069 | 0.195 |
MOD_PKA_2 | 237 | 243 | PF00069 | 0.419 |
MOD_PKA_2 | 303 | 309 | PF00069 | 0.407 |
MOD_PKA_2 | 380 | 386 | PF00069 | 0.464 |
MOD_PKB_1 | 302 | 310 | PF00069 | 0.215 |
MOD_Plk_2-3 | 130 | 136 | PF00069 | 0.289 |
MOD_Plk_4 | 109 | 115 | PF00069 | 0.347 |
MOD_Plk_4 | 177 | 183 | PF00069 | 0.240 |
MOD_Plk_4 | 198 | 204 | PF00069 | 0.360 |
MOD_Plk_4 | 335 | 341 | PF00069 | 0.272 |
MOD_Plk_4 | 356 | 362 | PF00069 | 0.299 |
MOD_Plk_4 | 372 | 378 | PF00069 | 0.280 |
MOD_Plk_4 | 380 | 386 | PF00069 | 0.417 |
MOD_Plk_4 | 69 | 75 | PF00069 | 0.415 |
MOD_ProDKin_1 | 185 | 191 | PF00069 | 0.320 |
MOD_ProDKin_1 | 329 | 335 | PF00069 | 0.257 |
MOD_ProDKin_1 | 58 | 64 | PF00069 | 0.294 |
MOD_ProDKin_1 | 8 | 14 | PF00069 | 0.577 |
MOD_SUMO_rev_2 | 93 | 102 | PF00179 | 0.159 |
TRG_AP2beta_CARGO_1 | 140 | 149 | PF09066 | 0.195 |
TRG_DiLeu_BaEn_4 | 225 | 231 | PF01217 | 0.412 |
TRG_ENDOCYTIC_2 | 118 | 121 | PF00928 | 0.266 |
TRG_ENDOCYTIC_2 | 384 | 387 | PF00928 | 0.456 |
TRG_ENDOCYTIC_2 | 42 | 45 | PF00928 | 0.334 |
TRG_ENDOCYTIC_2 | 80 | 83 | PF00928 | 0.333 |
TRG_ER_diArg_1 | 148 | 151 | PF00400 | 0.218 |
TRG_ER_diArg_1 | 19 | 22 | PF00400 | 0.333 |
TRG_ER_diArg_1 | 227 | 230 | PF00400 | 0.370 |
TRG_ER_diArg_1 | 301 | 304 | PF00400 | 0.379 |
TRG_Pf-PMV_PEXEL_1 | 126 | 130 | PF00026 | 0.353 |
TRG_PTS1 | 428 | 431 | PF00515 | 0.681 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3D3 | Leptomonas seymouri | 65% | 100% |
A0A0N0P3S4 | Leptomonas seymouri | 36% | 100% |
A0A0N1PA10 | Leptomonas seymouri | 30% | 100% |
A0A0N1PCQ2 | Leptomonas seymouri | 32% | 100% |
A0A0S4JQB3 | Bodo saltans | 30% | 100% |
A0A1X0NSR3 | Trypanosomatidae | 29% | 96% |
A0A1X0NSS6 | Trypanosomatidae | 33% | 100% |
A0A1X0NT85 | Trypanosomatidae | 33% | 87% |
A0A3Q8IAY1 | Leishmania donovani | 38% | 100% |
A0A3R7KKJ0 | Trypanosoma rangeli | 33% | 100% |
A0A3S5IRR1 | Trypanosoma rangeli | 37% | 100% |
A0A3S7WUJ3 | Leishmania donovani | 31% | 91% |
A0A3S7X1K2 | Leishmania donovani | 31% | 100% |
A0A422NS41 | Trypanosoma rangeli | 30% | 100% |
A4H956 | Leishmania braziliensis | 33% | 95% |
A4H959 | Leishmania braziliensis | 79% | 99% |
A4H960 | Leishmania braziliensis | 37% | 100% |
A4HGL0 | Leishmania braziliensis | 29% | 87% |
A4HXH8 | Leishmania infantum | 31% | 91% |
A4HXI1 | Leishmania infantum | 99% | 100% |
A4HXI2 | Leishmania infantum | 38% | 100% |
A4I3N6 | Leishmania infantum | 32% | 96% |
C9ZP69 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
C9ZP70 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
E9AR73 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 86% |
E9AR76 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
E9AR77 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 37% | 96% |
E9AZX7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 96% |
Q4Q8A8 | Leishmania major | 31% | 96% |
Q4QE86 | Leishmania major | 37% | 100% |
Q4QE87 | Leishmania major | 93% | 100% |
Q4QE90 | Leishmania major | 37% | 100% |
Q54528 | Streptomyces purpurascens | 26% | 100% |
Q54809 | Streptomyces peucetius | 27% | 100% |
Q55217 | Streptomyces sp. (strain C5) | 27% | 100% |
V5AZB9 | Trypanosoma cruzi | 31% | 100% |
V5BER0 | Trypanosoma cruzi | 32% | 100% |
V5BNU9 | Trypanosoma cruzi | 34% | 100% |