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: 33 |
NetGPI | no | yes: 0, no: 33 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 16 |
GO:0110165 | cellular anatomical entity | 1 | 16 |
Related structures:
AlphaFold database: Q4QI90
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 265 | 267 | PF00675 | 0.455 |
CLV_NRD_NRD_1 | 39 | 41 | PF00675 | 0.390 |
CLV_NRD_NRD_1 | 474 | 476 | PF00675 | 0.508 |
CLV_NRD_NRD_1 | 68 | 70 | PF00675 | 0.373 |
CLV_NRD_NRD_1 | 7 | 9 | PF00675 | 0.487 |
CLV_PCSK_FUR_1 | 263 | 267 | PF00082 | 0.380 |
CLV_PCSK_FUR_1 | 5 | 9 | PF00082 | 0.368 |
CLV_PCSK_KEX2_1 | 265 | 267 | PF00082 | 0.435 |
CLV_PCSK_KEX2_1 | 39 | 41 | PF00082 | 0.389 |
CLV_PCSK_KEX2_1 | 474 | 476 | PF00082 | 0.508 |
CLV_PCSK_KEX2_1 | 582 | 584 | PF00082 | 0.568 |
CLV_PCSK_KEX2_1 | 68 | 70 | PF00082 | 0.372 |
CLV_PCSK_KEX2_1 | 7 | 9 | PF00082 | 0.494 |
CLV_PCSK_PC1ET2_1 | 582 | 584 | PF00082 | 0.591 |
CLV_PCSK_SKI1_1 | 131 | 135 | PF00082 | 0.312 |
CLV_PCSK_SKI1_1 | 225 | 229 | PF00082 | 0.384 |
CLV_PCSK_SKI1_1 | 359 | 363 | PF00082 | 0.589 |
CLV_PCSK_SKI1_1 | 440 | 444 | PF00082 | 0.636 |
CLV_PCSK_SKI1_1 | 559 | 563 | PF00082 | 0.495 |
CLV_PCSK_SKI1_1 | 8 | 12 | PF00082 | 0.427 |
DEG_Kelch_actinfilin_1 | 447 | 451 | PF01344 | 0.227 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.616 |
DEG_SCF_FBW7_1 | 488 | 493 | PF00400 | 0.251 |
DEG_SPOP_SBC_1 | 333 | 337 | PF00917 | 0.498 |
DOC_CYCLIN_RxL_1 | 5 | 15 | PF00134 | 0.593 |
DOC_MAPK_gen_1 | 209 | 218 | PF00069 | 0.550 |
DOC_MAPK_gen_1 | 474 | 481 | PF00069 | 0.277 |
DOC_MAPK_gen_1 | 68 | 74 | PF00069 | 0.539 |
DOC_MAPK_MEF2A_6 | 446 | 454 | PF00069 | 0.328 |
DOC_MAPK_MEF2A_6 | 474 | 483 | PF00069 | 0.303 |
DOC_PP1_RVXF_1 | 181 | 188 | PF00149 | 0.449 |
DOC_PP1_RVXF_1 | 495 | 501 | PF00149 | 0.341 |
DOC_PP1_RVXF_1 | 606 | 613 | PF00149 | 0.315 |
DOC_PP2B_LxvP_1 | 159 | 162 | PF13499 | 0.512 |
DOC_PP2B_LxvP_1 | 417 | 420 | PF13499 | 0.370 |
DOC_PP2B_PxIxI_1 | 369 | 375 | PF00149 | 0.296 |
DOC_PP4_FxxP_1 | 43 | 46 | PF00568 | 0.659 |
DOC_SPAK_OSR1_1 | 306 | 310 | PF12202 | 0.374 |
DOC_USP7_MATH_1 | 13 | 17 | PF00917 | 0.628 |
DOC_USP7_MATH_1 | 22 | 26 | PF00917 | 0.700 |
DOC_USP7_MATH_1 | 234 | 238 | PF00917 | 0.564 |
DOC_USP7_MATH_1 | 484 | 488 | PF00917 | 0.294 |
DOC_USP7_MATH_2 | 552 | 558 | PF00917 | 0.263 |
DOC_USP7_UBL2_3 | 310 | 314 | PF12436 | 0.365 |
DOC_USP7_UBL2_3 | 578 | 582 | PF12436 | 0.360 |
DOC_WW_Pin1_4 | 486 | 491 | PF00397 | 0.363 |
DOC_WW_Pin1_4 | 548 | 553 | PF00397 | 0.364 |
LIG_14-3-3_CanoR_1 | 235 | 239 | PF00244 | 0.515 |
LIG_14-3-3_CanoR_1 | 265 | 275 | PF00244 | 0.613 |
LIG_14-3-3_CanoR_1 | 294 | 303 | PF00244 | 0.436 |
LIG_14-3-3_CanoR_1 | 344 | 353 | PF00244 | 0.381 |
LIG_14-3-3_CanoR_1 | 39 | 44 | PF00244 | 0.672 |
LIG_14-3-3_CanoR_1 | 565 | 575 | PF00244 | 0.408 |
LIG_14-3-3_CanoR_1 | 8 | 18 | PF00244 | 0.640 |
LIG_Actin_WH2_2 | 169 | 185 | PF00022 | 0.474 |
LIG_Actin_WH2_2 | 396 | 413 | PF00022 | 0.359 |
LIG_APCC_ABBA_1 | 524 | 529 | PF00400 | 0.339 |
LIG_BIR_III_4 | 520 | 524 | PF00653 | 0.275 |
LIG_BRCT_BRCA1_1 | 278 | 282 | PF00533 | 0.270 |
LIG_BRCT_BRCA1_1 | 82 | 86 | PF00533 | 0.603 |
LIG_deltaCOP1_diTrp_1 | 355 | 362 | PF00928 | 0.358 |
LIG_deltaCOP1_diTrp_1 | 618 | 622 | PF00928 | 0.315 |
LIG_EH1_1 | 132 | 140 | PF00400 | 0.474 |
LIG_eIF4E_1 | 555 | 561 | PF01652 | 0.317 |
LIG_FHA_1 | 130 | 136 | PF00498 | 0.585 |
LIG_FHA_1 | 145 | 151 | PF00498 | 0.560 |
LIG_FHA_1 | 167 | 173 | PF00498 | 0.568 |
LIG_FHA_1 | 194 | 200 | PF00498 | 0.509 |
LIG_FHA_1 | 489 | 495 | PF00498 | 0.426 |
LIG_FHA_2 | 329 | 335 | PF00498 | 0.609 |
LIG_LIR_Apic_2 | 41 | 46 | PF02991 | 0.665 |
LIG_LIR_Apic_2 | 499 | 504 | PF02991 | 0.356 |
LIG_LIR_Gen_1 | 509 | 519 | PF02991 | 0.362 |
LIG_LIR_Nem_3 | 103 | 109 | PF02991 | 0.549 |
LIG_LIR_Nem_3 | 269 | 275 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 499 | 503 | PF02991 | 0.334 |
LIG_LIR_Nem_3 | 509 | 515 | PF02991 | 0.340 |
LIG_NRBOX | 147 | 153 | PF00104 | 0.460 |
LIG_NRBOX | 537 | 543 | PF00104 | 0.331 |
LIG_Pex14_2 | 282 | 286 | PF04695 | 0.317 |
LIG_Pex14_2 | 86 | 90 | PF04695 | 0.595 |
LIG_SH2_CRK | 272 | 276 | PF00017 | 0.277 |
LIG_SH2_CRK | 501 | 505 | PF00017 | 0.363 |
LIG_SH2_CRK | 613 | 617 | PF00017 | 0.353 |
LIG_SH2_NCK_1 | 501 | 505 | PF00017 | 0.315 |
LIG_SH2_NCK_1 | 613 | 617 | PF00017 | 0.348 |
LIG_SH2_SRC | 512 | 515 | PF00017 | 0.410 |
LIG_SH2_SRC | 589 | 592 | PF00017 | 0.323 |
LIG_SH2_STAT3 | 555 | 558 | PF00017 | 0.303 |
LIG_SH2_STAT5 | 106 | 109 | PF00017 | 0.533 |
LIG_SH2_STAT5 | 181 | 184 | PF00017 | 0.532 |
LIG_SH2_STAT5 | 217 | 220 | PF00017 | 0.553 |
LIG_SH2_STAT5 | 296 | 299 | PF00017 | 0.380 |
LIG_SH2_STAT5 | 378 | 381 | PF00017 | 0.340 |
LIG_SH2_STAT5 | 501 | 504 | PF00017 | 0.364 |
LIG_SH2_STAT5 | 514 | 517 | PF00017 | 0.338 |
LIG_SH2_STAT5 | 555 | 558 | PF00017 | 0.365 |
LIG_SH3_3 | 478 | 484 | PF00018 | 0.333 |
LIG_SH3_3 | 55 | 61 | PF00018 | 0.653 |
LIG_SUMO_SIM_par_1 | 371 | 376 | PF11976 | 0.290 |
LIG_TYR_ITIM | 611 | 616 | PF00017 | 0.324 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.596 |
MOD_CK1_1 | 336 | 342 | PF00069 | 0.532 |
MOD_CK1_1 | 97 | 103 | PF00069 | 0.703 |
MOD_CK2_1 | 234 | 240 | PF00069 | 0.545 |
MOD_CK2_1 | 328 | 334 | PF00069 | 0.626 |
MOD_CK2_1 | 548 | 554 | PF00069 | 0.386 |
MOD_GlcNHglycan | 125 | 128 | PF01048 | 0.564 |
MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.354 |
MOD_GlcNHglycan | 193 | 196 | PF01048 | 0.352 |
MOD_GlcNHglycan | 232 | 235 | PF01048 | 0.325 |
MOD_GlcNHglycan | 268 | 271 | PF01048 | 0.348 |
MOD_GlcNHglycan | 276 | 279 | PF01048 | 0.280 |
MOD_GlcNHglycan | 324 | 327 | PF01048 | 0.703 |
MOD_GlcNHglycan | 339 | 342 | PF01048 | 0.668 |
MOD_GlcNHglycan | 35 | 38 | PF01048 | 0.510 |
MOD_GlcNHglycan | 96 | 99 | PF01048 | 0.321 |
MOD_GSK3_1 | 17 | 24 | PF00069 | 0.673 |
MOD_GSK3_1 | 187 | 194 | PF00069 | 0.499 |
MOD_GSK3_1 | 219 | 226 | PF00069 | 0.513 |
MOD_GSK3_1 | 230 | 237 | PF00069 | 0.474 |
MOD_GSK3_1 | 295 | 302 | PF00069 | 0.411 |
MOD_GSK3_1 | 328 | 335 | PF00069 | 0.548 |
MOD_GSK3_1 | 339 | 346 | PF00069 | 0.511 |
MOD_GSK3_1 | 382 | 389 | PF00069 | 0.322 |
MOD_GSK3_1 | 484 | 491 | PF00069 | 0.302 |
MOD_GSK3_1 | 550 | 557 | PF00069 | 0.462 |
MOD_GSK3_1 | 9 | 16 | PF00069 | 0.649 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.558 |
MOD_N-GLC_1 | 129 | 134 | PF02516 | 0.418 |
MOD_N-GLC_1 | 144 | 149 | PF02516 | 0.366 |
MOD_N-GLC_1 | 18 | 23 | PF02516 | 0.440 |
MOD_N-GLC_1 | 504 | 509 | PF02516 | 0.541 |
MOD_NEK2_1 | 129 | 134 | PF00069 | 0.703 |
MOD_NEK2_1 | 230 | 235 | PF00069 | 0.509 |
MOD_NEK2_1 | 276 | 281 | PF00069 | 0.337 |
MOD_NEK2_1 | 386 | 391 | PF00069 | 0.284 |
MOD_NEK2_1 | 506 | 511 | PF00069 | 0.363 |
MOD_NEK2_1 | 527 | 532 | PF00069 | 0.323 |
MOD_NEK2_1 | 597 | 602 | PF00069 | 0.329 |
MOD_NEK2_1 | 612 | 617 | PF00069 | 0.350 |
MOD_NEK2_1 | 90 | 95 | PF00069 | 0.613 |
MOD_NEK2_2 | 284 | 289 | PF00069 | 0.286 |
MOD_PIKK_1 | 115 | 121 | PF00454 | 0.691 |
MOD_PIKK_1 | 228 | 234 | PF00454 | 0.496 |
MOD_PIKK_1 | 506 | 512 | PF00454 | 0.351 |
MOD_PIKK_1 | 554 | 560 | PF00454 | 0.252 |
MOD_PIKK_1 | 63 | 69 | PF00454 | 0.574 |
MOD_PK_1 | 438 | 444 | PF00069 | 0.265 |
MOD_PKA_1 | 39 | 45 | PF00069 | 0.548 |
MOD_PKA_2 | 234 | 240 | PF00069 | 0.519 |
MOD_PKA_2 | 343 | 349 | PF00069 | 0.404 |
MOD_PKA_2 | 38 | 44 | PF00069 | 0.574 |
MOD_Plk_1 | 129 | 135 | PF00069 | 0.700 |
MOD_Plk_1 | 406 | 412 | PF00069 | 0.415 |
MOD_Plk_1 | 597 | 603 | PF00069 | 0.320 |
MOD_Plk_4 | 234 | 240 | PF00069 | 0.507 |
MOD_Plk_4 | 490 | 496 | PF00069 | 0.286 |
MOD_Plk_4 | 80 | 86 | PF00069 | 0.537 |
MOD_ProDKin_1 | 486 | 492 | PF00069 | 0.359 |
MOD_ProDKin_1 | 548 | 554 | PF00069 | 0.365 |
TRG_DiLeu_BaEn_1 | 214 | 219 | PF01217 | 0.534 |
TRG_ENDOCYTIC_2 | 181 | 184 | PF00928 | 0.523 |
TRG_ENDOCYTIC_2 | 272 | 275 | PF00928 | 0.298 |
TRG_ENDOCYTIC_2 | 512 | 515 | PF00928 | 0.354 |
TRG_ENDOCYTIC_2 | 613 | 616 | PF00928 | 0.347 |
TRG_ER_diArg_1 | 265 | 267 | PF00400 | 0.659 |
TRG_ER_diArg_1 | 38 | 40 | PF00400 | 0.633 |
TRG_ER_diArg_1 | 5 | 8 | PF00400 | 0.716 |
TRG_ER_diArg_1 | 68 | 70 | PF00400 | 0.676 |
TRG_NES_CRM1_1 | 408 | 423 | PF08389 | 0.358 |
TRG_NES_CRM1_1 | 513 | 525 | PF08389 | 0.363 |
TRG_Pf-PMV_PEXEL_1 | 356 | 360 | PF00026 | 0.524 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PAN2 | Leptomonas seymouri | 42% | 97% |
A0A0N1PB02 | Leptomonas seymouri | 49% | 97% |
A0A0S4J6C6 | Bodo saltans | 44% | 98% |
A0A1X0P9A6 | Trypanosomatidae | 43% | 93% |
A0A3Q8IHH1 | Leishmania donovani | 36% | 87% |
A0A3R7K2Y9 | Trypanosoma rangeli | 49% | 93% |
A0A3S5H668 | Leishmania donovani | 47% | 100% |
A0A3S5H669 | Leishmania donovani | 94% | 100% |
A0A3S7X835 | Leishmania donovani | 46% | 100% |
A4H5C9 | Leishmania braziliensis | 44% | 100% |
A4H5D0 | Leishmania braziliensis | 73% | 100% |
A4HAZ7 | Leishmania braziliensis | 42% | 100% |
A4HAZ9 | Leishmania braziliensis | 43% | 100% |
A4HB01 | Leishmania braziliensis | 43% | 100% |
A4HTM0 | Leishmania infantum | 47% | 100% |
A4HTM1 | Leishmania infantum | 94% | 100% |
A4IA57 | Leishmania infantum | 46% | 100% |
C6K3V8 | Leptomonas seymouri | 44% | 100% |
C6K3V9 | Leptomonas seymouri | 71% | 97% |
C9ZMY5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 49% | 94% |
E8NHE5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
E8NHF8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 100% |
E9AME6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 47% | 100% |
E9AME7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
E9B571 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 45% | 100% |
Q4Q1U8 | Leishmania major | 38% | 100% |
Q4Q2R4 | Leishmania major | 46% | 99% |
Q4Q310 | Leishmania major | 38% | 100% |
Q4Q312 | Leishmania major | 37% | 100% |
Q4Q340 | Leishmania major | 38% | 100% |
Q4Q342 | Leishmania major | 38% | 100% |
Q4QI91 | Leishmania major | 47% | 100% |