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: 8 |
NetGPI | no | yes: 0, no: 8 |
Related structures:
AlphaFold database: A0A3Q8IHV3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 265 | 269 | PF00656 | 0.501 |
CLV_NRD_NRD_1 | 230 | 232 | PF00675 | 0.511 |
CLV_NRD_NRD_1 | 261 | 263 | PF00675 | 0.453 |
CLV_NRD_NRD_1 | 353 | 355 | PF00675 | 0.354 |
CLV_NRD_NRD_1 | 473 | 475 | PF00675 | 0.246 |
CLV_PCSK_KEX2_1 | 229 | 231 | PF00082 | 0.511 |
CLV_PCSK_KEX2_1 | 261 | 263 | PF00082 | 0.540 |
CLV_PCSK_KEX2_1 | 353 | 355 | PF00082 | 0.383 |
CLV_PCSK_KEX2_1 | 369 | 371 | PF00082 | 0.389 |
CLV_PCSK_KEX2_1 | 400 | 402 | PF00082 | 0.324 |
CLV_PCSK_KEX2_1 | 84 | 86 | PF00082 | 0.565 |
CLV_PCSK_PC1ET2_1 | 369 | 371 | PF00082 | 0.343 |
CLV_PCSK_PC1ET2_1 | 400 | 402 | PF00082 | 0.336 |
CLV_PCSK_PC1ET2_1 | 84 | 86 | PF00082 | 0.544 |
CLV_PCSK_PC7_1 | 225 | 231 | PF00082 | 0.581 |
CLV_PCSK_SKI1_1 | 176 | 180 | PF00082 | 0.367 |
CLV_PCSK_SKI1_1 | 191 | 195 | PF00082 | 0.409 |
CLV_PCSK_SKI1_1 | 369 | 373 | PF00082 | 0.361 |
CLV_PCSK_SKI1_1 | 56 | 60 | PF00082 | 0.470 |
CLV_PCSK_SKI1_1 | 81 | 85 | PF00082 | 0.516 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.712 |
DOC_CKS1_1 | 127 | 132 | PF01111 | 0.629 |
DOC_CYCLIN_RxL_1 | 173 | 182 | PF00134 | 0.524 |
DOC_CYCLIN_yCln2_LP_2 | 426 | 432 | PF00134 | 0.421 |
DOC_MAPK_gen_1 | 21 | 28 | PF00069 | 0.417 |
DOC_MAPK_gen_1 | 81 | 90 | PF00069 | 0.508 |
DOC_PP2B_LxvP_1 | 237 | 240 | PF13499 | 0.409 |
DOC_PP2B_LxvP_1 | 426 | 429 | PF13499 | 0.421 |
DOC_PP2B_LxvP_1 | 495 | 498 | PF13499 | 0.331 |
DOC_PP4_FxxP_1 | 422 | 425 | PF00568 | 0.460 |
DOC_USP7_MATH_1 | 161 | 165 | PF00917 | 0.627 |
DOC_USP7_MATH_1 | 168 | 172 | PF00917 | 0.603 |
DOC_USP7_MATH_1 | 328 | 332 | PF00917 | 0.324 |
DOC_USP7_MATH_1 | 348 | 352 | PF00917 | 0.336 |
DOC_USP7_MATH_1 | 40 | 44 | PF00917 | 0.519 |
DOC_USP7_MATH_1 | 73 | 77 | PF00917 | 0.513 |
DOC_USP7_UBL2_3 | 481 | 485 | PF12436 | 0.348 |
DOC_WW_Pin1_4 | 126 | 131 | PF00397 | 0.604 |
DOC_WW_Pin1_4 | 282 | 287 | PF00397 | 0.494 |
DOC_WW_Pin1_4 | 421 | 426 | PF00397 | 0.382 |
DOC_WW_Pin1_4 | 59 | 64 | PF00397 | 0.579 |
LIG_14-3-3_CanoR_1 | 21 | 27 | PF00244 | 0.535 |
LIG_14-3-3_CanoR_1 | 280 | 286 | PF00244 | 0.502 |
LIG_14-3-3_CanoR_1 | 330 | 336 | PF00244 | 0.406 |
LIG_14-3-3_CanoR_1 | 74 | 80 | PF00244 | 0.459 |
LIG_BRCT_BRCA1_1 | 214 | 218 | PF00533 | 0.462 |
LIG_BRCT_BRCA1_1 | 483 | 487 | PF00533 | 0.406 |
LIG_Clathr_ClatBox_1 | 416 | 420 | PF01394 | 0.362 |
LIG_deltaCOP1_diTrp_1 | 125 | 131 | PF00928 | 0.487 |
LIG_deltaCOP1_diTrp_1 | 209 | 218 | PF00928 | 0.471 |
LIG_deltaCOP1_diTrp_1 | 377 | 382 | PF00928 | 0.324 |
LIG_FHA_1 | 134 | 140 | PF00498 | 0.562 |
LIG_FHA_1 | 172 | 178 | PF00498 | 0.493 |
LIG_FHA_1 | 23 | 29 | PF00498 | 0.414 |
LIG_FHA_1 | 301 | 307 | PF00498 | 0.365 |
LIG_FHA_1 | 43 | 49 | PF00498 | 0.460 |
LIG_FHA_2 | 154 | 160 | PF00498 | 0.676 |
LIG_FHA_2 | 198 | 204 | PF00498 | 0.564 |
LIG_FHA_2 | 222 | 228 | PF00498 | 0.576 |
LIG_FHA_2 | 254 | 260 | PF00498 | 0.446 |
LIG_LIR_Apic_2 | 125 | 130 | PF02991 | 0.587 |
LIG_LIR_Apic_2 | 420 | 425 | PF02991 | 0.460 |
LIG_LIR_Gen_1 | 114 | 124 | PF02991 | 0.580 |
LIG_LIR_Gen_1 | 381 | 388 | PF02991 | 0.324 |
LIG_LIR_Gen_1 | 452 | 462 | PF02991 | 0.406 |
LIG_LIR_Nem_3 | 114 | 120 | PF02991 | 0.577 |
LIG_LIR_Nem_3 | 255 | 260 | PF02991 | 0.499 |
LIG_LIR_Nem_3 | 307 | 313 | PF02991 | 0.319 |
LIG_LIR_Nem_3 | 452 | 458 | PF02991 | 0.406 |
LIG_LIR_Nem_3 | 459 | 465 | PF02991 | 0.406 |
LIG_MLH1_MIPbox_1 | 483 | 487 | PF16413 | 0.406 |
LIG_PCNA_PIPBox_1 | 385 | 394 | PF02747 | 0.460 |
LIG_PCNA_PIPBox_1 | 415 | 424 | PF02747 | 0.324 |
LIG_Pex14_1 | 127 | 131 | PF04695 | 0.536 |
LIG_Pex14_1 | 325 | 329 | PF04695 | 0.324 |
LIG_Pex14_1 | 378 | 382 | PF04695 | 0.324 |
LIG_SH2_CRK | 241 | 245 | PF00017 | 0.497 |
LIG_SH2_CRK | 329 | 333 | PF00017 | 0.350 |
LIG_SH2_STAP1 | 437 | 441 | PF00017 | 0.324 |
LIG_SH2_STAT3 | 465 | 468 | PF00017 | 0.460 |
LIG_SH2_STAT5 | 391 | 394 | PF00017 | 0.406 |
LIG_SH2_STAT5 | 455 | 458 | PF00017 | 0.324 |
LIG_SH2_STAT5 | 477 | 480 | PF00017 | 0.358 |
LIG_SH3_3 | 144 | 150 | PF00018 | 0.548 |
LIG_SH3_3 | 207 | 213 | PF00018 | 0.393 |
LIG_SH3_3 | 293 | 299 | PF00018 | 0.547 |
LIG_SUMO_SIM_anti_2 | 383 | 388 | PF11976 | 0.324 |
LIG_SUMO_SIM_par_1 | 302 | 307 | PF11976 | 0.396 |
LIG_SUMO_SIM_par_1 | 415 | 420 | PF11976 | 0.285 |
LIG_TYR_ITIM | 239 | 244 | PF00017 | 0.506 |
LIG_WRC_WIRS_1 | 379 | 384 | PF05994 | 0.324 |
MOD_CDC14_SPxK_1 | 285 | 288 | PF00782 | 0.464 |
MOD_CDK_SPxK_1 | 282 | 288 | PF00069 | 0.465 |
MOD_CK1_1 | 108 | 114 | PF00069 | 0.522 |
MOD_CK1_1 | 135 | 141 | PF00069 | 0.441 |
MOD_CK1_1 | 171 | 177 | PF00069 | 0.546 |
MOD_CK1_1 | 294 | 300 | PF00069 | 0.532 |
MOD_CK1_1 | 331 | 337 | PF00069 | 0.324 |
MOD_CK1_1 | 42 | 48 | PF00069 | 0.493 |
MOD_CK2_1 | 108 | 114 | PF00069 | 0.562 |
MOD_CK2_1 | 142 | 148 | PF00069 | 0.591 |
MOD_CK2_1 | 179 | 185 | PF00069 | 0.434 |
MOD_CK2_1 | 197 | 203 | PF00069 | 0.330 |
MOD_CK2_1 | 48 | 54 | PF00069 | 0.470 |
MOD_CMANNOS | 254 | 257 | PF00535 | 0.491 |
MOD_GlcNHglycan | 121 | 125 | PF01048 | 0.510 |
MOD_GlcNHglycan | 163 | 166 | PF01048 | 0.627 |
MOD_GlcNHglycan | 181 | 184 | PF01048 | 0.305 |
MOD_GlcNHglycan | 293 | 296 | PF01048 | 0.479 |
MOD_GlcNHglycan | 306 | 309 | PF01048 | 0.271 |
MOD_GlcNHglycan | 462 | 465 | PF01048 | 0.406 |
MOD_GlcNHglycan | 50 | 53 | PF01048 | 0.533 |
MOD_GlcNHglycan | 99 | 102 | PF01048 | 0.563 |
MOD_GSK3_1 | 105 | 112 | PF00069 | 0.612 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.557 |
MOD_GSK3_1 | 149 | 156 | PF00069 | 0.604 |
MOD_GSK3_1 | 168 | 175 | PF00069 | 0.548 |
MOD_GSK3_1 | 197 | 204 | PF00069 | 0.553 |
MOD_GSK3_1 | 267 | 274 | PF00069 | 0.531 |
MOD_GSK3_1 | 300 | 307 | PF00069 | 0.366 |
MOD_GSK3_1 | 433 | 440 | PF00069 | 0.299 |
MOD_GSK3_1 | 460 | 467 | PF00069 | 0.326 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.431 |
MOD_N-GLC_1 | 91 | 96 | PF02516 | 0.402 |
MOD_N-GLC_2 | 494 | 496 | PF02516 | 0.324 |
MOD_NEK2_1 | 172 | 177 | PF00069 | 0.464 |
MOD_NEK2_1 | 179 | 184 | PF00069 | 0.371 |
MOD_NEK2_1 | 304 | 309 | PF00069 | 0.360 |
MOD_NEK2_1 | 39 | 44 | PF00069 | 0.411 |
MOD_NEK2_1 | 395 | 400 | PF00069 | 0.329 |
MOD_NEK2_1 | 48 | 53 | PF00069 | 0.434 |
MOD_NEK2_1 | 79 | 84 | PF00069 | 0.503 |
MOD_OFUCOSY | 72 | 77 | PF10250 | 0.420 |
MOD_PIKK_1 | 464 | 470 | PF00454 | 0.406 |
MOD_PK_1 | 267 | 273 | PF00069 | 0.447 |
MOD_PKA_2 | 73 | 79 | PF00069 | 0.439 |
MOD_Plk_1 | 108 | 114 | PF00069 | 0.589 |
MOD_Plk_1 | 168 | 174 | PF00069 | 0.516 |
MOD_Plk_1 | 267 | 273 | PF00069 | 0.506 |
MOD_Plk_1 | 395 | 401 | PF00069 | 0.303 |
MOD_Plk_1 | 410 | 416 | PF00069 | 0.375 |
MOD_Plk_2-3 | 109 | 115 | PF00069 | 0.492 |
MOD_Plk_4 | 112 | 118 | PF00069 | 0.574 |
MOD_Plk_4 | 168 | 174 | PF00069 | 0.569 |
MOD_Plk_4 | 212 | 218 | PF00069 | 0.545 |
MOD_Plk_4 | 267 | 273 | PF00069 | 0.545 |
MOD_Plk_4 | 300 | 306 | PF00069 | 0.406 |
MOD_Plk_4 | 331 | 337 | PF00069 | 0.324 |
MOD_Plk_4 | 437 | 443 | PF00069 | 0.324 |
MOD_ProDKin_1 | 126 | 132 | PF00069 | 0.615 |
MOD_ProDKin_1 | 282 | 288 | PF00069 | 0.504 |
MOD_ProDKin_1 | 421 | 427 | PF00069 | 0.382 |
MOD_ProDKin_1 | 59 | 65 | PF00069 | 0.576 |
MOD_SUMO_rev_2 | 259 | 269 | PF00179 | 0.408 |
MOD_SUMO_rev_2 | 51 | 58 | PF00179 | 0.457 |
TRG_DiLeu_BaEn_1 | 452 | 457 | PF01217 | 0.324 |
TRG_DiLeu_BaEn_2 | 53 | 59 | PF01217 | 0.495 |
TRG_ENDOCYTIC_2 | 241 | 244 | PF00928 | 0.502 |
TRG_ENDOCYTIC_2 | 329 | 332 | PF00928 | 0.345 |
TRG_ENDOCYTIC_2 | 455 | 458 | PF00928 | 0.406 |
TRG_ER_diArg_1 | 229 | 231 | PF00400 | 0.512 |
TRG_ER_diArg_1 | 260 | 262 | PF00400 | 0.434 |
TRG_ER_diArg_1 | 352 | 354 | PF00400 | 0.389 |
TRG_NES_CRM1_1 | 377 | 390 | PF08389 | 0.324 |
TRG_Pf-PMV_PEXEL_1 | 176 | 181 | PF00026 | 0.498 |
TRG_Pf-PMV_PEXEL_1 | 191 | 196 | PF00026 | 0.380 |
TRG_Pf-PMV_PEXEL_1 | 353 | 357 | PF00026 | 0.366 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I0K1 | Leptomonas seymouri | 59% | 99% |
A0A1X0PB53 | Trypanosomatidae | 43% | 100% |
A4HBC3 | Leishmania braziliensis | 78% | 100% |
A4IAH1 | Leishmania infantum | 99% | 100% |
C9ZLS0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
E9B5J5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
Q4Q2E1 | Leishmania major | 91% | 100% |
Q5XIB4 | Rattus norvegicus | 33% | 100% |