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: A4H959
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 34 |
GO:0016787 | hydrolase activity | 2 | 34 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 94 | 98 | PF00656 | 0.340 |
CLV_NRD_NRD_1 | 404 | 406 | PF00675 | 0.571 |
CLV_PCSK_KEX2_1 | 276 | 278 | PF00082 | 0.248 |
CLV_PCSK_PC1ET2_1 | 276 | 278 | PF00082 | 0.297 |
CLV_PCSK_SKI1_1 | 269 | 273 | PF00082 | 0.305 |
CLV_PCSK_SKI1_1 | 286 | 290 | PF00082 | 0.310 |
DEG_APCC_DBOX_1 | 285 | 293 | PF00400 | 0.391 |
DEG_SPOP_SBC_1 | 207 | 211 | PF00917 | 0.400 |
DEG_SPOP_SBC_1 | 414 | 418 | PF00917 | 0.429 |
DOC_CKS1_1 | 4 | 9 | PF01111 | 0.434 |
DOC_MAPK_gen_1 | 273 | 281 | PF00069 | 0.358 |
DOC_MAPK_gen_1 | 302 | 310 | PF00069 | 0.311 |
DOC_MAPK_MEF2A_6 | 49 | 57 | PF00069 | 0.288 |
DOC_PP2B_LxvP_1 | 10 | 13 | PF13499 | 0.723 |
DOC_PP2B_LxvP_1 | 292 | 295 | PF13499 | 0.346 |
DOC_PP2B_LxvP_1 | 335 | 338 | PF13499 | 0.237 |
DOC_PP2B_PxIxI_1 | 337 | 343 | PF00149 | 0.204 |
DOC_USP7_MATH_1 | 413 | 417 | PF00917 | 0.633 |
DOC_USP7_UBL2_3 | 248 | 252 | PF12436 | 0.373 |
DOC_WW_Pin1_4 | 185 | 190 | PF00397 | 0.318 |
DOC_WW_Pin1_4 | 220 | 225 | PF00397 | 0.459 |
DOC_WW_Pin1_4 | 3 | 8 | PF00397 | 0.660 |
DOC_WW_Pin1_4 | 330 | 335 | PF00397 | 0.240 |
DOC_WW_Pin1_4 | 47 | 52 | PF00397 | 0.424 |
DOC_WW_Pin1_4 | 58 | 63 | PF00397 | 0.321 |
LIG_14-3-3_CanoR_1 | 175 | 182 | PF00244 | 0.286 |
LIG_14-3-3_CanoR_1 | 30 | 38 | PF00244 | 0.410 |
LIG_14-3-3_CanoR_1 | 302 | 310 | PF00244 | 0.328 |
LIG_14-3-3_CanoR_1 | 324 | 334 | PF00244 | 0.452 |
LIG_14-3-3_CanoR_1 | 356 | 362 | PF00244 | 0.316 |
LIG_14-3-3_CanoR_1 | 382 | 386 | PF00244 | 0.236 |
LIG_Actin_WH2_2 | 366 | 384 | PF00022 | 0.147 |
LIG_APCC_ABBA_1 | 169 | 174 | PF00400 | 0.147 |
LIG_APCC_ABBA_1 | 239 | 244 | PF00400 | 0.147 |
LIG_APCC_ABBAyCdc20_2 | 238 | 244 | PF00400 | 0.147 |
LIG_BIR_III_4 | 140 | 144 | PF00653 | 0.402 |
LIG_BRCT_BRCA1_1 | 21 | 25 | PF00533 | 0.515 |
LIG_FHA_1 | 109 | 115 | PF00498 | 0.428 |
LIG_FHA_1 | 123 | 129 | PF00498 | 0.414 |
LIG_FHA_1 | 337 | 343 | PF00498 | 0.241 |
LIG_FHA_1 | 4 | 10 | PF00498 | 0.502 |
LIG_FHA_2 | 125 | 131 | PF00498 | 0.288 |
LIG_FHA_2 | 193 | 199 | PF00498 | 0.147 |
LIG_FHA_2 | 92 | 98 | PF00498 | 0.324 |
LIG_LIR_Gen_1 | 201 | 207 | PF02991 | 0.407 |
LIG_LIR_Gen_1 | 244 | 253 | PF02991 | 0.401 |
LIG_LIR_Gen_1 | 261 | 267 | PF02991 | 0.460 |
LIG_LIR_Gen_1 | 384 | 393 | PF02991 | 0.401 |
LIG_LIR_Gen_1 | 77 | 85 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 110 | 116 | PF02991 | 0.312 |
LIG_LIR_Nem_3 | 140 | 145 | PF02991 | 0.386 |
LIG_LIR_Nem_3 | 201 | 205 | PF02991 | 0.373 |
LIG_LIR_Nem_3 | 244 | 249 | PF02991 | 0.425 |
LIG_LIR_Nem_3 | 261 | 265 | PF02991 | 0.269 |
LIG_LIR_Nem_3 | 384 | 388 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 44 | 48 | PF02991 | 0.358 |
LIG_LIR_Nem_3 | 77 | 83 | PF02991 | 0.299 |
LIG_NRBOX | 69 | 75 | PF00104 | 0.249 |
LIG_PDZ_Class_1 | 424 | 429 | PF00595 | 0.694 |
LIG_SH2_CRK | 118 | 122 | PF00017 | 0.306 |
LIG_SH2_CRK | 80 | 84 | PF00017 | 0.474 |
LIG_SH2_GRB2like | 280 | 283 | PF00017 | 0.156 |
LIG_SH2_PTP2 | 385 | 388 | PF00017 | 0.483 |
LIG_SH2_SRC | 116 | 119 | PF00017 | 0.204 |
LIG_SH2_SRC | 242 | 245 | PF00017 | 0.147 |
LIG_SH2_SRC | 280 | 283 | PF00017 | 0.232 |
LIG_SH2_STAP1 | 116 | 120 | PF00017 | 0.406 |
LIG_SH2_STAP1 | 214 | 218 | PF00017 | 0.399 |
LIG_SH2_STAP1 | 242 | 246 | PF00017 | 0.400 |
LIG_SH2_STAP1 | 260 | 264 | PF00017 | 0.274 |
LIG_SH2_STAT5 | 113 | 116 | PF00017 | 0.400 |
LIG_SH2_STAT5 | 132 | 135 | PF00017 | 0.306 |
LIG_SH2_STAT5 | 280 | 283 | PF00017 | 0.246 |
LIG_SH2_STAT5 | 336 | 339 | PF00017 | 0.377 |
LIG_SH2_STAT5 | 385 | 388 | PF00017 | 0.460 |
LIG_SH3_3 | 15 | 21 | PF00018 | 0.604 |
LIG_SH3_3 | 345 | 351 | PF00018 | 0.282 |
LIG_SH3_3 | 45 | 51 | PF00018 | 0.414 |
LIG_SUMO_SIM_anti_2 | 201 | 207 | PF11976 | 0.418 |
LIG_SxIP_EBH_1 | 356 | 368 | PF03271 | 0.206 |
LIG_TRAF2_1 | 223 | 226 | PF00917 | 0.400 |
LIG_UBA3_1 | 199 | 208 | PF00899 | 0.352 |
LIG_WRC_WIRS_1 | 199 | 204 | PF05994 | 0.269 |
LIG_WRC_WIRS_1 | 42 | 47 | PF05994 | 0.300 |
MOD_CDK_SPxxK_3 | 220 | 227 | PF00069 | 0.147 |
MOD_CK1_1 | 107 | 113 | PF00069 | 0.307 |
MOD_CK1_1 | 183 | 189 | PF00069 | 0.285 |
MOD_CK1_1 | 201 | 207 | PF00069 | 0.214 |
MOD_CK1_1 | 258 | 264 | PF00069 | 0.251 |
MOD_CK1_1 | 416 | 422 | PF00069 | 0.709 |
MOD_CK1_1 | 5 | 11 | PF00069 | 0.698 |
MOD_CK2_1 | 124 | 130 | PF00069 | 0.339 |
MOD_CK2_1 | 220 | 226 | PF00069 | 0.369 |
MOD_Cter_Amidation | 403 | 406 | PF01082 | 0.414 |
MOD_DYRK1A_RPxSP_1 | 220 | 224 | PF00069 | 0.147 |
MOD_GlcNHglycan | 210 | 213 | PF01048 | 0.375 |
MOD_GlcNHglycan | 253 | 256 | PF01048 | 0.349 |
MOD_GlcNHglycan | 328 | 331 | PF01048 | 0.412 |
MOD_GlcNHglycan | 409 | 412 | PF01048 | 0.590 |
MOD_GlcNHglycan | 76 | 79 | PF01048 | 0.453 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.313 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.266 |
MOD_GSK3_1 | 251 | 258 | PF00069 | 0.366 |
MOD_GSK3_1 | 304 | 311 | PF00069 | 0.350 |
MOD_GSK3_1 | 320 | 327 | PF00069 | 0.415 |
MOD_N-GLC_1 | 320 | 325 | PF02516 | 0.207 |
MOD_NEK2_1 | 108 | 113 | PF00069 | 0.396 |
MOD_NEK2_1 | 155 | 160 | PF00069 | 0.336 |
MOD_NEK2_1 | 177 | 182 | PF00069 | 0.276 |
MOD_NEK2_1 | 275 | 280 | PF00069 | 0.299 |
MOD_NEK2_1 | 373 | 378 | PF00069 | 0.380 |
MOD_NEK2_1 | 381 | 386 | PF00069 | 0.384 |
MOD_NEK2_1 | 74 | 79 | PF00069 | 0.407 |
MOD_NEK2_2 | 124 | 129 | PF00069 | 0.204 |
MOD_PIKK_1 | 175 | 181 | PF00454 | 0.373 |
MOD_PIKK_1 | 308 | 314 | PF00454 | 0.451 |
MOD_PK_1 | 304 | 310 | PF00069 | 0.406 |
MOD_PKA_2 | 19 | 25 | PF00069 | 0.363 |
MOD_PKA_2 | 303 | 309 | PF00069 | 0.395 |
MOD_PKA_2 | 31 | 37 | PF00069 | 0.425 |
MOD_PKA_2 | 381 | 387 | PF00069 | 0.449 |
MOD_PKA_2 | 91 | 97 | PF00069 | 0.313 |
MOD_PKB_1 | 302 | 310 | PF00069 | 0.204 |
MOD_Plk_2-3 | 130 | 136 | PF00069 | 0.270 |
MOD_Plk_4 | 109 | 115 | PF00069 | 0.372 |
MOD_Plk_4 | 14 | 20 | PF00069 | 0.354 |
MOD_Plk_4 | 164 | 170 | PF00069 | 0.265 |
MOD_Plk_4 | 177 | 183 | PF00069 | 0.246 |
MOD_Plk_4 | 198 | 204 | PF00069 | 0.361 |
MOD_Plk_4 | 336 | 342 | PF00069 | 0.281 |
MOD_Plk_4 | 357 | 363 | PF00069 | 0.314 |
MOD_Plk_4 | 373 | 379 | PF00069 | 0.373 |
MOD_Plk_4 | 381 | 387 | PF00069 | 0.390 |
MOD_Plk_4 | 5 | 11 | PF00069 | 0.540 |
MOD_Plk_4 | 69 | 75 | PF00069 | 0.411 |
MOD_ProDKin_1 | 185 | 191 | PF00069 | 0.318 |
MOD_ProDKin_1 | 220 | 226 | PF00069 | 0.459 |
MOD_ProDKin_1 | 3 | 9 | PF00069 | 0.660 |
MOD_ProDKin_1 | 330 | 336 | PF00069 | 0.240 |
MOD_ProDKin_1 | 47 | 53 | PF00069 | 0.415 |
MOD_ProDKin_1 | 58 | 64 | PF00069 | 0.321 |
MOD_SUMO_for_1 | 212 | 215 | PF00179 | 0.147 |
TRG_DiLeu_BaEn_4 | 225 | 231 | PF01217 | 0.400 |
TRG_ENDOCYTIC_2 | 118 | 121 | PF00928 | 0.281 |
TRG_ENDOCYTIC_2 | 385 | 388 | PF00928 | 0.500 |
TRG_ENDOCYTIC_2 | 42 | 45 | PF00928 | 0.312 |
TRG_ENDOCYTIC_2 | 80 | 83 | PF00928 | 0.328 |
TRG_ER_diArg_1 | 227 | 230 | PF00400 | 0.370 |
TRG_ER_diArg_1 | 301 | 304 | PF00400 | 0.368 |
TRG_ER_diArg_1 | 37 | 40 | PF00400 | 0.434 |
TRG_ER_diArg_1 | 402 | 405 | PF00400 | 0.548 |
TRG_NES_CRM1_1 | 299 | 313 | PF08389 | 0.142 |
TRG_Pf-PMV_PEXEL_1 | 126 | 130 | PF00026 | 0.327 |
TRG_Pf-PMV_PEXEL_1 | 175 | 179 | PF00026 | 0.147 |
TRG_Pf-PMV_PEXEL_1 | 387 | 391 | PF00026 | 0.493 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3D3 | Leptomonas seymouri | 65% | 100% |
A0A0N0P3S4 | Leptomonas seymouri | 34% | 100% |
A0A0N1PA10 | Leptomonas seymouri | 29% | 100% |
A0A0N1PCQ2 | Leptomonas seymouri | 30% | 100% |
A0A0S4JQB3 | Bodo saltans | 31% | 100% |
A0A0S4KKL9 | Bodo saltans | 27% | 81% |
A0A1X0NSR3 | Trypanosomatidae | 31% | 96% |
A0A1X0NSS6 | Trypanosomatidae | 31% | 100% |
A0A1X0NT85 | Trypanosomatidae | 32% | 87% |
A0A3Q8IAY1 | Leishmania donovani | 36% | 100% |
A0A3S5IRR1 | Trypanosoma rangeli | 39% | 100% |
A0A3S7WUJ3 | Leishmania donovani | 30% | 100% |
A0A3S7WUK0 | Leishmania donovani | 79% | 100% |
A0A3S7X1K2 | Leishmania donovani | 31% | 100% |
A0A422NS41 | Trypanosoma rangeli | 31% | 100% |
A4H956 | Leishmania braziliensis | 33% | 89% |
A4H960 | Leishmania braziliensis | 36% | 100% |
A4HGL0 | Leishmania braziliensis | 31% | 100% |
A4HXH8 | Leishmania infantum | 31% | 100% |
A4HXI1 | Leishmania infantum | 79% | 100% |
A4HXI2 | Leishmania infantum | 36% | 100% |
A4I3N6 | Leishmania infantum | 31% | 100% |
C9ZP69 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
C9ZP70 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
E9AR73 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
E9AR76 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 99% |
E9AR77 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 100% |
E9AZX7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
Q4Q8A8 | Leishmania major | 31% | 95% |
Q4QE86 | Leishmania major | 36% | 100% |
Q4QE87 | Leishmania major | 77% | 100% |
Q4QE90 | Leishmania major | 31% | 90% |
Q54528 | Streptomyces purpurascens | 26% | 100% |
V5AZB9 | Trypanosoma cruzi | 31% | 100% |
V5BER0 | Trypanosoma cruzi | 32% | 100% |
V5BNU9 | Trypanosoma cruzi | 33% | 100% |