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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 2 |
GO:0016020 | membrane | 2 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
Related structures:
AlphaFold database: Q4QC26
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 158 | 160 | PF00675 | 0.381 |
CLV_NRD_NRD_1 | 174 | 176 | PF00675 | 0.195 |
CLV_NRD_NRD_1 | 249 | 251 | PF00675 | 0.365 |
CLV_NRD_NRD_1 | 281 | 283 | PF00675 | 0.597 |
CLV_PCSK_FUR_1 | 172 | 176 | PF00082 | 0.400 |
CLV_PCSK_FUR_1 | 247 | 251 | PF00082 | 0.436 |
CLV_PCSK_KEX2_1 | 158 | 160 | PF00082 | 0.383 |
CLV_PCSK_KEX2_1 | 172 | 174 | PF00082 | 0.277 |
CLV_PCSK_KEX2_1 | 249 | 251 | PF00082 | 0.409 |
CLV_PCSK_KEX2_1 | 37 | 39 | PF00082 | 0.462 |
CLV_PCSK_KEX2_1 | 94 | 96 | PF00082 | 0.390 |
CLV_PCSK_PC1ET2_1 | 37 | 39 | PF00082 | 0.482 |
CLV_PCSK_PC1ET2_1 | 94 | 96 | PF00082 | 0.390 |
CLV_PCSK_SKI1_1 | 147 | 151 | PF00082 | 0.448 |
CLV_PCSK_SKI1_1 | 175 | 179 | PF00082 | 0.355 |
CLV_PCSK_SKI1_1 | 48 | 52 | PF00082 | 0.355 |
CLV_Separin_Metazoa | 447 | 451 | PF03568 | 0.610 |
DEG_APCC_DBOX_1 | 47 | 55 | PF00400 | 0.548 |
DEG_MDM2_SWIB_1 | 215 | 223 | PF02201 | 0.427 |
DEG_MDM2_SWIB_1 | 286 | 293 | PF02201 | 0.333 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.715 |
DEG_SPOP_SBC_1 | 9 | 13 | PF00917 | 0.702 |
DOC_CDC14_PxL_1 | 239 | 247 | PF14671 | 0.633 |
DOC_CKS1_1 | 461 | 466 | PF01111 | 0.629 |
DOC_CYCLIN_RxL_1 | 247 | 258 | PF00134 | 0.613 |
DOC_MAPK_DCC_7 | 94 | 104 | PF00069 | 0.651 |
DOC_MAPK_gen_1 | 172 | 180 | PF00069 | 0.528 |
DOC_MAPK_gen_1 | 247 | 256 | PF00069 | 0.573 |
DOC_MAPK_gen_1 | 392 | 400 | PF00069 | 0.539 |
DOC_MAPK_gen_1 | 45 | 54 | PF00069 | 0.526 |
DOC_MAPK_MEF2A_6 | 172 | 180 | PF00069 | 0.517 |
DOC_MAPK_MEF2A_6 | 394 | 402 | PF00069 | 0.544 |
DOC_MAPK_MEF2A_6 | 45 | 54 | PF00069 | 0.548 |
DOC_PP1_RVXF_1 | 250 | 257 | PF00149 | 0.497 |
DOC_PP1_RVXF_1 | 36 | 43 | PF00149 | 0.549 |
DOC_PP2B_LxvP_1 | 142 | 145 | PF13499 | 0.626 |
DOC_PP2B_LxvP_1 | 336 | 339 | PF13499 | 0.341 |
DOC_SPAK_OSR1_1 | 332 | 336 | PF12202 | 0.406 |
DOC_USP7_MATH_1 | 143 | 147 | PF00917 | 0.687 |
DOC_USP7_MATH_1 | 347 | 351 | PF00917 | 0.427 |
DOC_USP7_UBL2_3 | 152 | 156 | PF12436 | 0.633 |
DOC_WW_Pin1_4 | 460 | 465 | PF00397 | 0.623 |
LIG_14-3-3_CanoR_1 | 285 | 289 | PF00244 | 0.386 |
LIG_14-3-3_CanoR_1 | 319 | 327 | PF00244 | 0.632 |
LIG_14-3-3_CanoR_1 | 38 | 43 | PF00244 | 0.641 |
LIG_14-3-3_CanoR_1 | 438 | 448 | PF00244 | 0.429 |
LIG_APCC_ABBA_1 | 52 | 57 | PF00400 | 0.548 |
LIG_BRCT_BRCA1_1 | 10 | 14 | PF00533 | 0.683 |
LIG_EH1_1 | 407 | 415 | PF00400 | 0.356 |
LIG_eIF4E_1 | 361 | 367 | PF01652 | 0.352 |
LIG_FHA_1 | 203 | 209 | PF00498 | 0.411 |
LIG_FHA_1 | 259 | 265 | PF00498 | 0.340 |
LIG_FHA_1 | 271 | 277 | PF00498 | 0.252 |
LIG_FHA_1 | 292 | 298 | PF00498 | 0.348 |
LIG_FHA_1 | 4 | 10 | PF00498 | 0.751 |
LIG_GBD_Chelix_1 | 189 | 197 | PF00786 | 0.420 |
LIG_GBD_Chelix_1 | 396 | 404 | PF00786 | 0.494 |
LIG_LIR_Gen_1 | 284 | 293 | PF02991 | 0.316 |
LIG_LIR_Gen_1 | 350 | 359 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 11 | 17 | PF02991 | 0.603 |
LIG_LIR_Nem_3 | 163 | 169 | PF02991 | 0.564 |
LIG_LIR_Nem_3 | 212 | 218 | PF02991 | 0.275 |
LIG_LIR_Nem_3 | 284 | 289 | PF02991 | 0.339 |
LIG_LIR_Nem_3 | 329 | 334 | PF02991 | 0.575 |
LIG_LIR_Nem_3 | 350 | 354 | PF02991 | 0.363 |
LIG_LIR_Nem_3 | 386 | 390 | PF02991 | 0.603 |
LIG_LIR_Nem_3 | 416 | 420 | PF02991 | 0.339 |
LIG_LIR_Nem_3 | 64 | 69 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 78 | 82 | PF02991 | 0.350 |
LIG_LYPXL_S_1 | 99 | 103 | PF13949 | 0.419 |
LIG_LYPXL_yS_3 | 100 | 103 | PF13949 | 0.566 |
LIG_NRBOX | 380 | 386 | PF00104 | 0.349 |
LIG_Pex14_2 | 10 | 14 | PF04695 | 0.570 |
LIG_Pex14_2 | 215 | 219 | PF04695 | 0.321 |
LIG_Pex14_2 | 286 | 290 | PF04695 | 0.290 |
LIG_Pex14_2 | 342 | 346 | PF04695 | 0.380 |
LIG_Pex14_2 | 383 | 387 | PF04695 | 0.412 |
LIG_Pex14_2 | 430 | 434 | PF04695 | 0.354 |
LIG_RPA_C_Fungi | 433 | 445 | PF08784 | 0.356 |
LIG_SH2_CRK | 112 | 116 | PF00017 | 0.540 |
LIG_SH2_CRK | 167 | 171 | PF00017 | 0.475 |
LIG_SH2_NCK_1 | 112 | 116 | PF00017 | 0.584 |
LIG_SH2_STAT5 | 169 | 172 | PF00017 | 0.415 |
LIG_SH2_STAT5 | 222 | 225 | PF00017 | 0.321 |
LIG_SH2_STAT5 | 356 | 359 | PF00017 | 0.419 |
LIG_SH2_STAT5 | 364 | 367 | PF00017 | 0.321 |
LIG_SH2_STAT5 | 439 | 442 | PF00017 | 0.456 |
LIG_SH2_STAT5 | 91 | 94 | PF00017 | 0.503 |
LIG_SH3_3 | 135 | 141 | PF00018 | 0.643 |
LIG_SH3_3 | 95 | 101 | PF00018 | 0.447 |
LIG_SUMO_SIM_anti_2 | 258 | 264 | PF11976 | 0.358 |
LIG_SUMO_SIM_par_1 | 293 | 298 | PF11976 | 0.427 |
LIG_SUMO_SIM_par_1 | 370 | 375 | PF11976 | 0.348 |
LIG_TYR_ITIM | 134 | 139 | PF00017 | 0.641 |
LIG_TYR_ITIM | 98 | 103 | PF00017 | 0.456 |
LIG_UBA3_1 | 244 | 252 | PF00899 | 0.459 |
LIG_UBA3_1 | 274 | 283 | PF00899 | 0.504 |
LIG_WRC_WIRS_1 | 14 | 19 | PF05994 | 0.466 |
LIG_WRC_WIRS_1 | 296 | 301 | PF05994 | 0.427 |
MOD_CK1_1 | 13 | 19 | PF00069 | 0.537 |
MOD_CK1_1 | 258 | 264 | PF00069 | 0.385 |
MOD_CK2_1 | 17 | 23 | PF00069 | 0.700 |
MOD_CK2_1 | 38 | 44 | PF00069 | 0.606 |
MOD_Cter_Amidation | 280 | 283 | PF01082 | 0.463 |
MOD_GlcNHglycan | 257 | 260 | PF01048 | 0.325 |
MOD_GlcNHglycan | 442 | 445 | PF01048 | 0.427 |
MOD_GSK3_1 | 291 | 298 | PF00069 | 0.346 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.394 |
MOD_GSK3_1 | 9 | 16 | PF00069 | 0.550 |
MOD_N-GLC_1 | 209 | 214 | PF02516 | 0.427 |
MOD_N-GLC_2 | 457 | 459 | PF02516 | 0.500 |
MOD_NEK2_1 | 10 | 15 | PF00069 | 0.596 |
MOD_NEK2_1 | 180 | 185 | PF00069 | 0.308 |
MOD_NEK2_1 | 191 | 196 | PF00069 | 0.290 |
MOD_NEK2_1 | 208 | 213 | PF00069 | 0.317 |
MOD_NEK2_1 | 448 | 453 | PF00069 | 0.473 |
MOD_PIKK_1 | 113 | 119 | PF00454 | 0.617 |
MOD_PIKK_1 | 160 | 166 | PF00454 | 0.604 |
MOD_PKA_2 | 160 | 166 | PF00069 | 0.502 |
MOD_PKA_2 | 284 | 290 | PF00069 | 0.492 |
MOD_Plk_1 | 209 | 215 | PF00069 | 0.482 |
MOD_Plk_2-3 | 23 | 29 | PF00069 | 0.488 |
MOD_Plk_4 | 13 | 19 | PF00069 | 0.603 |
MOD_Plk_4 | 182 | 188 | PF00069 | 0.368 |
MOD_Plk_4 | 209 | 215 | PF00069 | 0.408 |
MOD_Plk_4 | 258 | 264 | PF00069 | 0.358 |
MOD_Plk_4 | 270 | 276 | PF00069 | 0.249 |
MOD_Plk_4 | 38 | 44 | PF00069 | 0.457 |
MOD_ProDKin_1 | 460 | 466 | PF00069 | 0.535 |
TRG_DiLeu_BaEn_2 | 328 | 334 | PF01217 | 0.534 |
TRG_DiLeu_BaLyEn_6 | 121 | 126 | PF01217 | 0.598 |
TRG_DiLeu_LyEn_5 | 240 | 245 | PF01217 | 0.512 |
TRG_ENDOCYTIC_2 | 100 | 103 | PF00928 | 0.452 |
TRG_ENDOCYTIC_2 | 112 | 115 | PF00928 | 0.490 |
TRG_ENDOCYTIC_2 | 136 | 139 | PF00928 | 0.642 |
TRG_ENDOCYTIC_2 | 167 | 170 | PF00928 | 0.420 |
TRG_ENDOCYTIC_2 | 222 | 225 | PF00928 | 0.311 |
TRG_ENDOCYTIC_2 | 305 | 308 | PF00928 | 0.321 |
TRG_ENDOCYTIC_2 | 364 | 367 | PF00928 | 0.321 |
TRG_ER_diArg_1 | 122 | 125 | PF00400 | 0.515 |
TRG_ER_diArg_1 | 157 | 159 | PF00400 | 0.512 |
TRG_ER_diArg_1 | 172 | 175 | PF00400 | 0.341 |
TRG_ER_diArg_1 | 246 | 249 | PF00400 | 0.455 |
TRG_NES_CRM1_1 | 316 | 329 | PF08389 | 0.545 |
TRG_NES_CRM1_1 | 44 | 57 | PF08389 | 0.420 |
TRG_Pf-PMV_PEXEL_1 | 124 | 129 | PF00026 | 0.623 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HVU0 | Leptomonas seymouri | 76% | 100% |
A0A0S4JHL9 | Bodo saltans | 29% | 70% |
A0A1X0NI23 | Trypanosomatidae | 51% | 100% |
A0A3Q8IAZ7 | Leishmania donovani | 96% | 100% |
A0A422N8A5 | Trypanosoma rangeli | 48% | 100% |
A4HC20 | Leishmania braziliensis | 85% | 100% |
A4HZJ5 | Leishmania infantum | 96% | 100% |
D0A112 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 98% |
E9AVF3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |