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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: Q4QGD6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 316 | 320 | PF00656 | 0.504 |
CLV_C14_Caspase3-7 | 82 | 86 | PF00656 | 0.699 |
CLV_NRD_NRD_1 | 184 | 186 | PF00675 | 0.605 |
CLV_NRD_NRD_1 | 298 | 300 | PF00675 | 0.478 |
CLV_NRD_NRD_1 | 359 | 361 | PF00675 | 0.307 |
CLV_PCSK_KEX2_1 | 184 | 186 | PF00082 | 0.605 |
CLV_PCSK_KEX2_1 | 297 | 299 | PF00082 | 0.505 |
CLV_PCSK_KEX2_1 | 358 | 360 | PF00082 | 0.308 |
CLV_PCSK_SKI1_1 | 175 | 179 | PF00082 | 0.455 |
CLV_PCSK_SKI1_1 | 256 | 260 | PF00082 | 0.354 |
CLV_PCSK_SKI1_1 | 325 | 329 | PF00082 | 0.373 |
CLV_PCSK_SKI1_1 | 376 | 380 | PF00082 | 0.350 |
CLV_PCSK_SKI1_1 | 390 | 394 | PF00082 | 0.245 |
DEG_APCC_DBOX_1 | 255 | 263 | PF00400 | 0.342 |
DEG_APCC_DBOX_1 | 289 | 297 | PF00400 | 0.399 |
DEG_Nend_UBRbox_4 | 1 | 3 | PF02207 | 0.560 |
DEG_SCF_FBW7_1 | 405 | 411 | PF00400 | 0.532 |
DEG_SPOP_SBC_1 | 219 | 223 | PF00917 | 0.623 |
DEG_SPOP_SBC_1 | 409 | 413 | PF00917 | 0.539 |
DOC_ANK_TNKS_1 | 394 | 401 | PF00023 | 0.215 |
DOC_CKS1_1 | 405 | 410 | PF01111 | 0.578 |
DOC_CYCLIN_RxL_1 | 250 | 261 | PF00134 | 0.454 |
DOC_CYCLIN_RxL_1 | 385 | 397 | PF00134 | 0.498 |
DOC_MAPK_MEF2A_6 | 21 | 28 | PF00069 | 0.422 |
DOC_MAPK_MEF2A_6 | 285 | 293 | PF00069 | 0.425 |
DOC_MAPK_NFAT4_5 | 21 | 29 | PF00069 | 0.411 |
DOC_PP2B_LxvP_1 | 252 | 255 | PF13499 | 0.485 |
DOC_USP7_MATH_1 | 10 | 14 | PF00917 | 0.508 |
DOC_USP7_MATH_1 | 159 | 163 | PF00917 | 0.519 |
DOC_USP7_MATH_1 | 219 | 223 | PF00917 | 0.593 |
DOC_USP7_MATH_1 | 224 | 228 | PF00917 | 0.543 |
DOC_USP7_MATH_1 | 410 | 414 | PF00917 | 0.588 |
DOC_USP7_MATH_1 | 83 | 87 | PF00917 | 0.538 |
DOC_WW_Pin1_4 | 183 | 188 | PF00397 | 0.563 |
DOC_WW_Pin1_4 | 226 | 231 | PF00397 | 0.639 |
DOC_WW_Pin1_4 | 401 | 406 | PF00397 | 0.571 |
DOC_WW_Pin1_4 | 59 | 64 | PF00397 | 0.592 |
LIG_14-3-3_CanoR_1 | 11 | 16 | PF00244 | 0.611 |
LIG_14-3-3_CanoR_1 | 127 | 136 | PF00244 | 0.361 |
LIG_14-3-3_CanoR_1 | 139 | 147 | PF00244 | 0.525 |
LIG_14-3-3_CanoR_1 | 21 | 27 | PF00244 | 0.390 |
LIG_14-3-3_CanoR_1 | 212 | 218 | PF00244 | 0.734 |
LIG_14-3-3_CanoR_1 | 247 | 253 | PF00244 | 0.468 |
LIG_BIR_III_2 | 402 | 406 | PF00653 | 0.488 |
LIG_CaM_IQ_9 | 277 | 292 | PF13499 | 0.365 |
LIG_CaM_NSCaTE_8 | 136 | 143 | PF13499 | 0.435 |
LIG_FHA_1 | 106 | 112 | PF00498 | 0.368 |
LIG_FHA_1 | 12 | 18 | PF00498 | 0.544 |
LIG_FHA_1 | 21 | 27 | PF00498 | 0.377 |
LIG_FHA_1 | 212 | 218 | PF00498 | 0.713 |
LIG_FHA_1 | 263 | 269 | PF00498 | 0.497 |
LIG_FHA_1 | 319 | 325 | PF00498 | 0.512 |
LIG_FHA_1 | 363 | 369 | PF00498 | 0.408 |
LIG_FHA_1 | 370 | 376 | PF00498 | 0.303 |
LIG_FHA_2 | 150 | 156 | PF00498 | 0.547 |
LIG_LIR_Apic_2 | 197 | 202 | PF02991 | 0.551 |
LIG_LIR_Gen_1 | 113 | 123 | PF02991 | 0.454 |
LIG_LIR_Gen_1 | 214 | 220 | PF02991 | 0.713 |
LIG_LIR_Nem_3 | 113 | 119 | PF02991 | 0.445 |
LIG_LIR_Nem_3 | 214 | 218 | PF02991 | 0.748 |
LIG_LYPXL_SIV_4 | 172 | 180 | PF13949 | 0.452 |
LIG_RPA_C_Fungi | 44 | 56 | PF08784 | 0.430 |
LIG_SH2_CRK | 116 | 120 | PF00017 | 0.461 |
LIG_SH2_CRK | 215 | 219 | PF00017 | 0.479 |
LIG_SH2_NCK_1 | 122 | 126 | PF00017 | 0.457 |
LIG_SH2_NCK_1 | 215 | 219 | PF00017 | 0.479 |
LIG_SH2_NCK_1 | 271 | 275 | PF00017 | 0.443 |
LIG_SH2_NCK_1 | 33 | 37 | PF00017 | 0.460 |
LIG_SH2_SRC | 122 | 125 | PF00017 | 0.453 |
LIG_SH2_SRC | 33 | 36 | PF00017 | 0.462 |
LIG_SH2_STAT3 | 415 | 418 | PF00017 | 0.522 |
LIG_SH2_STAT5 | 276 | 279 | PF00017 | 0.400 |
LIG_SH2_STAT5 | 361 | 364 | PF00017 | 0.284 |
LIG_SH3_1 | 184 | 190 | PF00018 | 0.508 |
LIG_SH3_1 | 361 | 367 | PF00018 | 0.284 |
LIG_SH3_3 | 184 | 190 | PF00018 | 0.508 |
LIG_SH3_3 | 197 | 203 | PF00018 | 0.642 |
LIG_SH3_3 | 361 | 367 | PF00018 | 0.284 |
LIG_SH3_3 | 402 | 408 | PF00018 | 0.646 |
LIG_SUMO_SIM_anti_2 | 108 | 114 | PF11976 | 0.338 |
LIG_SUMO_SIM_par_1 | 107 | 114 | PF11976 | 0.338 |
LIG_SUMO_SIM_par_1 | 53 | 60 | PF11976 | 0.491 |
LIG_SxIP_EBH_1 | 212 | 224 | PF03271 | 0.619 |
LIG_TRAF2_1 | 416 | 419 | PF00917 | 0.613 |
LIG_TRAF2_1 | 51 | 54 | PF00917 | 0.443 |
LIG_TRFH_1 | 215 | 219 | PF08558 | 0.479 |
LIG_TYR_ITIM | 213 | 218 | PF00017 | 0.478 |
LIG_WW_3 | 253 | 257 | PF00397 | 0.455 |
MOD_CK1_1 | 142 | 148 | PF00069 | 0.530 |
MOD_CK1_1 | 149 | 155 | PF00069 | 0.499 |
MOD_CK1_1 | 226 | 232 | PF00069 | 0.549 |
MOD_CK1_1 | 27 | 33 | PF00069 | 0.563 |
MOD_CK1_1 | 404 | 410 | PF00069 | 0.590 |
MOD_CK1_1 | 62 | 68 | PF00069 | 0.609 |
MOD_CK2_1 | 149 | 155 | PF00069 | 0.602 |
MOD_GlcNHglycan | 152 | 155 | PF01048 | 0.590 |
MOD_GlcNHglycan | 226 | 229 | PF01048 | 0.602 |
MOD_GlcNHglycan | 396 | 399 | PF01048 | 0.420 |
MOD_GlcNHglycan | 412 | 415 | PF01048 | 0.460 |
MOD_GSK3_1 | 138 | 145 | PF00069 | 0.510 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.477 |
MOD_GSK3_1 | 185 | 192 | PF00069 | 0.508 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.417 |
MOD_GSK3_1 | 219 | 226 | PF00069 | 0.651 |
MOD_GSK3_1 | 229 | 236 | PF00069 | 0.546 |
MOD_GSK3_1 | 350 | 357 | PF00069 | 0.400 |
MOD_GSK3_1 | 404 | 411 | PF00069 | 0.724 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.430 |
MOD_LATS_1 | 144 | 150 | PF00433 | 0.512 |
MOD_NEK2_1 | 105 | 110 | PF00069 | 0.374 |
MOD_NEK2_1 | 111 | 116 | PF00069 | 0.302 |
MOD_NEK2_1 | 140 | 145 | PF00069 | 0.523 |
MOD_NEK2_1 | 213 | 218 | PF00069 | 0.566 |
MOD_NEK2_1 | 220 | 225 | PF00069 | 0.526 |
MOD_NEK2_1 | 233 | 238 | PF00069 | 0.487 |
MOD_NEK2_1 | 24 | 29 | PF00069 | 0.425 |
MOD_NEK2_1 | 248 | 253 | PF00069 | 0.399 |
MOD_NEK2_1 | 350 | 355 | PF00069 | 0.440 |
MOD_NEK2_1 | 383 | 388 | PF00069 | 0.414 |
MOD_NEK2_1 | 57 | 62 | PF00069 | 0.505 |
MOD_PIKK_1 | 383 | 389 | PF00454 | 0.215 |
MOD_PIKK_1 | 91 | 97 | PF00454 | 0.527 |
MOD_PK_1 | 146 | 152 | PF00069 | 0.514 |
MOD_PKA_1 | 297 | 303 | PF00069 | 0.554 |
MOD_PKA_2 | 10 | 16 | PF00069 | 0.615 |
MOD_PKA_2 | 138 | 144 | PF00069 | 0.580 |
MOD_PKA_2 | 145 | 151 | PF00069 | 0.583 |
MOD_PKA_2 | 20 | 26 | PF00069 | 0.405 |
MOD_PKA_2 | 211 | 217 | PF00069 | 0.741 |
MOD_PKA_2 | 297 | 303 | PF00069 | 0.546 |
MOD_PKA_2 | 394 | 400 | PF00069 | 0.404 |
MOD_PKB_1 | 137 | 145 | PF00069 | 0.458 |
MOD_Plk_1 | 34 | 40 | PF00069 | 0.556 |
MOD_Plk_2-3 | 341 | 347 | PF00069 | 0.360 |
MOD_Plk_4 | 105 | 111 | PF00069 | 0.376 |
MOD_Plk_4 | 213 | 219 | PF00069 | 0.722 |
MOD_Plk_4 | 229 | 235 | PF00069 | 0.380 |
MOD_ProDKin_1 | 183 | 189 | PF00069 | 0.577 |
MOD_ProDKin_1 | 226 | 232 | PF00069 | 0.631 |
MOD_ProDKin_1 | 401 | 407 | PF00069 | 0.574 |
MOD_ProDKin_1 | 59 | 65 | PF00069 | 0.601 |
MOD_SUMO_rev_2 | 319 | 327 | PF00179 | 0.502 |
TRG_DiLeu_BaEn_1 | 124 | 129 | PF01217 | 0.380 |
TRG_DiLeu_BaEn_1 | 346 | 351 | PF01217 | 0.344 |
TRG_DiLeu_BaLyEn_6 | 335 | 340 | PF01217 | 0.400 |
TRG_DiLeu_LyEn_5 | 124 | 129 | PF01217 | 0.443 |
TRG_ENDOCYTIC_2 | 116 | 119 | PF00928 | 0.455 |
TRG_ENDOCYTIC_2 | 215 | 218 | PF00928 | 0.481 |
TRG_ENDOCYTIC_2 | 337 | 340 | PF00928 | 0.320 |
TRG_ER_diArg_1 | 101 | 104 | PF00400 | 0.461 |
TRG_ER_diArg_1 | 183 | 185 | PF00400 | 0.498 |
TRG_ER_diArg_1 | 296 | 299 | PF00400 | 0.548 |
TRG_ER_diArg_1 | 358 | 360 | PF00400 | 0.286 |
TRG_NES_CRM1_1 | 231 | 246 | PF08389 | 0.469 |
TRG_Pf-PMV_PEXEL_1 | 256 | 261 | PF00026 | 0.405 |
TRG_Pf-PMV_PEXEL_1 | 390 | 394 | PF00026 | 0.494 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PBN7 | Leptomonas seymouri | 47% | 100% |
A0A0S4JF77 | Bodo saltans | 31% | 85% |
A0A1X0NNA0 | Trypanosomatidae | 30% | 100% |
A0A3S7WSE7 | Leishmania donovani | 93% | 100% |
A0A422NP89 | Trypanosoma rangeli | 32% | 100% |
A4H725 | Leishmania braziliensis | 78% | 97% |
A4HVF4 | Leishmania infantum | 93% | 100% |
E9AP52 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 91% |