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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: Q4Q3Y8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 246 | 250 | PF00656 | 0.747 |
CLV_NRD_NRD_1 | 161 | 163 | PF00675 | 0.709 |
CLV_NRD_NRD_1 | 255 | 257 | PF00675 | 0.741 |
CLV_NRD_NRD_1 | 41 | 43 | PF00675 | 0.691 |
CLV_NRD_NRD_1 | 547 | 549 | PF00675 | 0.522 |
CLV_PCSK_KEX2_1 | 161 | 163 | PF00082 | 0.709 |
CLV_PCSK_KEX2_1 | 255 | 257 | PF00082 | 0.741 |
CLV_PCSK_KEX2_1 | 490 | 492 | PF00082 | 0.792 |
CLV_PCSK_KEX2_1 | 547 | 549 | PF00082 | 0.670 |
CLV_PCSK_KEX2_1 | 556 | 558 | PF00082 | 0.623 |
CLV_PCSK_PC1ET2_1 | 490 | 492 | PF00082 | 0.792 |
CLV_PCSK_PC1ET2_1 | 556 | 558 | PF00082 | 0.634 |
CLV_PCSK_SKI1_1 | 548 | 552 | PF00082 | 0.663 |
CLV_PCSK_SKI1_1 | 553 | 557 | PF00082 | 0.608 |
DEG_Nend_UBRbox_4 | 1 | 3 | PF02207 | 0.671 |
DEG_SPOP_SBC_1 | 215 | 219 | PF00917 | 0.737 |
DOC_CYCLIN_RxL_1 | 364 | 374 | PF00134 | 0.542 |
DOC_MAPK_gen_1 | 553 | 563 | PF00069 | 0.744 |
DOC_PP2B_LxvP_1 | 185 | 188 | PF13499 | 0.729 |
DOC_PP4_FxxP_1 | 438 | 441 | PF00568 | 0.540 |
DOC_USP7_MATH_1 | 169 | 173 | PF00917 | 0.691 |
DOC_USP7_MATH_1 | 213 | 217 | PF00917 | 0.721 |
DOC_USP7_MATH_1 | 22 | 26 | PF00917 | 0.606 |
DOC_USP7_MATH_1 | 237 | 241 | PF00917 | 0.728 |
DOC_USP7_MATH_1 | 333 | 337 | PF00917 | 0.818 |
DOC_USP7_MATH_1 | 344 | 348 | PF00917 | 0.623 |
DOC_USP7_MATH_1 | 350 | 354 | PF00917 | 0.518 |
DOC_USP7_MATH_1 | 412 | 416 | PF00917 | 0.731 |
DOC_USP7_MATH_1 | 421 | 425 | PF00917 | 0.513 |
DOC_USP7_MATH_1 | 67 | 71 | PF00917 | 0.738 |
DOC_USP7_MATH_2 | 456 | 462 | PF00917 | 0.625 |
DOC_USP7_UBL2_3 | 497 | 501 | PF12436 | 0.797 |
DOC_WW_Pin1_4 | 162 | 167 | PF00397 | 0.824 |
DOC_WW_Pin1_4 | 204 | 209 | PF00397 | 0.748 |
DOC_WW_Pin1_4 | 211 | 216 | PF00397 | 0.711 |
DOC_WW_Pin1_4 | 293 | 298 | PF00397 | 0.668 |
DOC_WW_Pin1_4 | 561 | 566 | PF00397 | 0.675 |
LIG_14-3-3_CanoR_1 | 132 | 140 | PF00244 | 0.637 |
LIG_14-3-3_CanoR_1 | 255 | 261 | PF00244 | 0.754 |
LIG_14-3-3_CanoR_1 | 525 | 534 | PF00244 | 0.741 |
LIG_BRCT_BRCA1_1 | 94 | 98 | PF00533 | 0.711 |
LIG_Clathr_ClatBox_1 | 279 | 283 | PF01394 | 0.702 |
LIG_eIF4E_1 | 391 | 397 | PF01652 | 0.522 |
LIG_FHA_1 | 178 | 184 | PF00498 | 0.734 |
LIG_FHA_1 | 225 | 231 | PF00498 | 0.769 |
LIG_FHA_1 | 243 | 249 | PF00498 | 0.537 |
LIG_FHA_1 | 379 | 385 | PF00498 | 0.574 |
LIG_FHA_2 | 134 | 140 | PF00498 | 0.740 |
LIG_FHA_2 | 145 | 151 | PF00498 | 0.609 |
LIG_FHA_2 | 398 | 404 | PF00498 | 0.624 |
LIG_Integrin_RGD_1 | 82 | 84 | PF01839 | 0.829 |
LIG_LIR_Apic_2 | 437 | 441 | PF02991 | 0.623 |
LIG_LIR_Apic_2 | 95 | 99 | PF02991 | 0.692 |
LIG_LIR_Gen_1 | 269 | 276 | PF02991 | 0.753 |
LIG_LIR_Nem_3 | 264 | 270 | PF02991 | 0.798 |
LIG_LIR_Nem_3 | 31 | 35 | PF02991 | 0.635 |
LIG_PCNA_yPIPBox_3 | 364 | 373 | PF02747 | 0.640 |
LIG_Pex14_2 | 438 | 442 | PF04695 | 0.578 |
LIG_SH2_NCK_1 | 238 | 242 | PF00017 | 0.691 |
LIG_SH2_STAP1 | 124 | 128 | PF00017 | 0.626 |
LIG_SH2_STAP1 | 238 | 242 | PF00017 | 0.691 |
LIG_SH2_STAT3 | 113 | 116 | PF00017 | 0.684 |
LIG_SH2_STAT5 | 113 | 116 | PF00017 | 0.643 |
LIG_SH2_STAT5 | 260 | 263 | PF00017 | 0.818 |
LIG_SH2_STAT5 | 32 | 35 | PF00017 | 0.567 |
LIG_SH2_STAT5 | 391 | 394 | PF00017 | 0.525 |
LIG_SH2_STAT5 | 7 | 10 | PF00017 | 0.666 |
LIG_SH3_3 | 111 | 117 | PF00018 | 0.595 |
LIG_SH3_3 | 181 | 187 | PF00018 | 0.754 |
LIG_SH3_3 | 450 | 456 | PF00018 | 0.814 |
LIG_SH3_3 | 472 | 478 | PF00018 | 0.746 |
LIG_SH3_3 | 534 | 540 | PF00018 | 0.568 |
LIG_SH3_3 | 61 | 67 | PF00018 | 0.727 |
LIG_SH3_3 | 71 | 77 | PF00018 | 0.627 |
LIG_SUMO_SIM_par_1 | 356 | 362 | PF11976 | 0.610 |
LIG_SUMO_SIM_par_1 | 368 | 374 | PF11976 | 0.444 |
LIG_SUMO_SIM_par_1 | 539 | 546 | PF11976 | 0.751 |
LIG_TRAF2_1 | 400 | 403 | PF00917 | 0.659 |
LIG_TYR_ITIM | 36 | 41 | PF00017 | 0.583 |
LIG_UBA3_1 | 551 | 556 | PF00899 | 0.736 |
LIG_WRC_WIRS_1 | 140 | 145 | PF05994 | 0.758 |
LIG_WRC_WIRS_1 | 226 | 231 | PF05994 | 0.553 |
LIG_WRC_WIRS_1 | 405 | 410 | PF05994 | 0.598 |
MOD_CK1_1 | 17 | 23 | PF00069 | 0.754 |
MOD_CK1_1 | 207 | 213 | PF00069 | 0.772 |
MOD_CK1_1 | 216 | 222 | PF00069 | 0.684 |
MOD_CK1_1 | 225 | 231 | PF00069 | 0.611 |
MOD_CK1_1 | 307 | 313 | PF00069 | 0.790 |
MOD_CK1_1 | 323 | 329 | PF00069 | 0.669 |
MOD_CK1_1 | 336 | 342 | PF00069 | 0.727 |
MOD_CK1_1 | 407 | 413 | PF00069 | 0.676 |
MOD_CK1_1 | 425 | 431 | PF00069 | 0.786 |
MOD_CK1_1 | 434 | 440 | PF00069 | 0.677 |
MOD_CK1_1 | 463 | 469 | PF00069 | 0.779 |
MOD_CK2_1 | 133 | 139 | PF00069 | 0.741 |
MOD_CK2_1 | 144 | 150 | PF00069 | 0.604 |
MOD_CK2_1 | 328 | 334 | PF00069 | 0.751 |
MOD_CK2_1 | 350 | 356 | PF00069 | 0.553 |
MOD_CK2_1 | 380 | 386 | PF00069 | 0.571 |
MOD_CK2_1 | 397 | 403 | PF00069 | 0.553 |
MOD_CK2_1 | 434 | 440 | PF00069 | 0.715 |
MOD_Cter_Amidation | 159 | 162 | PF01082 | 0.754 |
MOD_GlcNHglycan | 171 | 174 | PF01048 | 0.738 |
MOD_GlcNHglycan | 199 | 202 | PF01048 | 0.813 |
MOD_GlcNHglycan | 219 | 222 | PF01048 | 0.480 |
MOD_GlcNHglycan | 239 | 242 | PF01048 | 0.697 |
MOD_GlcNHglycan | 24 | 27 | PF01048 | 0.486 |
MOD_GlcNHglycan | 245 | 248 | PF01048 | 0.717 |
MOD_GlcNHglycan | 306 | 309 | PF01048 | 0.740 |
MOD_GlcNHglycan | 330 | 333 | PF01048 | 0.748 |
MOD_GlcNHglycan | 334 | 338 | PF01048 | 0.761 |
MOD_GlcNHglycan | 346 | 349 | PF01048 | 0.521 |
MOD_GlcNHglycan | 415 | 418 | PF01048 | 0.751 |
MOD_GlcNHglycan | 424 | 427 | PF01048 | 0.497 |
MOD_GlcNHglycan | 433 | 436 | PF01048 | 0.582 |
MOD_GlcNHglycan | 465 | 468 | PF01048 | 0.671 |
MOD_GlcNHglycan | 530 | 533 | PF01048 | 0.771 |
MOD_GlcNHglycan | 9 | 12 | PF01048 | 0.687 |
MOD_GSK3_1 | 167 | 174 | PF00069 | 0.677 |
MOD_GSK3_1 | 207 | 214 | PF00069 | 0.700 |
MOD_GSK3_1 | 215 | 222 | PF00069 | 0.715 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.697 |
MOD_GSK3_1 | 289 | 296 | PF00069 | 0.778 |
MOD_GSK3_1 | 303 | 310 | PF00069 | 0.646 |
MOD_GSK3_1 | 319 | 326 | PF00069 | 0.755 |
MOD_GSK3_1 | 404 | 411 | PF00069 | 0.605 |
MOD_GSK3_1 | 421 | 428 | PF00069 | 0.749 |
MOD_GSK3_1 | 430 | 437 | PF00069 | 0.796 |
MOD_GSK3_1 | 506 | 513 | PF00069 | 0.780 |
MOD_GSK3_1 | 524 | 531 | PF00069 | 0.668 |
MOD_GSK3_1 | 557 | 564 | PF00069 | 0.754 |
MOD_N-GLC_1 | 397 | 402 | PF02516 | 0.573 |
MOD_NEK2_1 | 154 | 159 | PF00069 | 0.816 |
MOD_NEK2_1 | 229 | 234 | PF00069 | 0.704 |
MOD_NEK2_1 | 378 | 383 | PF00069 | 0.594 |
MOD_NEK2_1 | 387 | 392 | PF00069 | 0.520 |
MOD_NEK2_1 | 408 | 413 | PF00069 | 0.596 |
MOD_NEK2_1 | 430 | 435 | PF00069 | 0.681 |
MOD_NEK2_1 | 56 | 61 | PF00069 | 0.572 |
MOD_NEK2_2 | 2 | 7 | PF00069 | 0.601 |
MOD_PIKK_1 | 289 | 295 | PF00454 | 0.719 |
MOD_PIKK_1 | 320 | 326 | PF00454 | 0.828 |
MOD_PIKK_1 | 378 | 384 | PF00454 | 0.588 |
MOD_PK_1 | 557 | 563 | PF00069 | 0.751 |
MOD_PKA_2 | 242 | 248 | PF00069 | 0.805 |
MOD_PKA_2 | 303 | 309 | PF00069 | 0.698 |
MOD_PKA_2 | 524 | 530 | PF00069 | 0.695 |
MOD_Plk_1 | 457 | 463 | PF00069 | 0.646 |
MOD_Plk_1 | 557 | 563 | PF00069 | 0.751 |
MOD_Plk_2-3 | 311 | 317 | PF00069 | 0.671 |
MOD_Plk_2-3 | 371 | 377 | PF00069 | 0.655 |
MOD_Plk_4 | 144 | 150 | PF00069 | 0.591 |
MOD_Plk_4 | 171 | 177 | PF00069 | 0.682 |
MOD_Plk_4 | 2 | 8 | PF00069 | 0.593 |
MOD_Plk_4 | 225 | 231 | PF00069 | 0.567 |
MOD_Plk_4 | 380 | 386 | PF00069 | 0.571 |
MOD_Plk_4 | 387 | 393 | PF00069 | 0.520 |
MOD_Plk_4 | 404 | 410 | PF00069 | 0.411 |
MOD_Plk_4 | 557 | 563 | PF00069 | 0.697 |
MOD_Plk_4 | 92 | 98 | PF00069 | 0.788 |
MOD_ProDKin_1 | 162 | 168 | PF00069 | 0.822 |
MOD_ProDKin_1 | 204 | 210 | PF00069 | 0.749 |
MOD_ProDKin_1 | 211 | 217 | PF00069 | 0.709 |
MOD_ProDKin_1 | 293 | 299 | PF00069 | 0.670 |
TRG_DiLeu_BaEn_2 | 276 | 282 | PF01217 | 0.601 |
TRG_DiLeu_BaLyEn_6 | 365 | 370 | PF01217 | 0.507 |
TRG_DiLeu_BaLyEn_6 | 442 | 447 | PF01217 | 0.689 |
TRG_DiLeu_BaLyEn_6 | 537 | 542 | PF01217 | 0.689 |
TRG_ENDOCYTIC_2 | 267 | 270 | PF00928 | 0.797 |
TRG_ENDOCYTIC_2 | 38 | 41 | PF00928 | 0.567 |
TRG_ER_diArg_1 | 161 | 164 | PF00400 | 0.711 |
TRG_ER_diArg_1 | 255 | 258 | PF00400 | 0.741 |
TRG_ER_diArg_1 | 547 | 549 | PF00400 | 0.522 |
TRG_NES_CRM1_1 | 277 | 290 | PF08389 | 0.719 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I2A9 | Leptomonas seymouri | 36% | 94% |
A0A3Q8IEY7 | Leishmania donovani | 88% | 99% |
A4HLR1 | Leishmania braziliensis | 69% | 99% |
A4I961 | Leishmania infantum | 89% | 88% |
E9B437 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 98% |