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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
Related structures:
AlphaFold database: A4HK86
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 135 | 139 | PF00656 | 0.613 |
CLV_C14_Caspase3-7 | 187 | 191 | PF00656 | 0.698 |
CLV_C14_Caspase3-7 | 347 | 351 | PF00656 | 0.580 |
CLV_C14_Caspase3-7 | 369 | 373 | PF00656 | 0.661 |
CLV_NRD_NRD_1 | 197 | 199 | PF00675 | 0.440 |
CLV_NRD_NRD_1 | 242 | 244 | PF00675 | 0.481 |
CLV_NRD_NRD_1 | 259 | 261 | PF00675 | 0.291 |
CLV_NRD_NRD_1 | 428 | 430 | PF00675 | 0.443 |
CLV_NRD_NRD_1 | 545 | 547 | PF00675 | 0.315 |
CLV_NRD_NRD_1 | 82 | 84 | PF00675 | 0.450 |
CLV_PCSK_KEX2_1 | 242 | 244 | PF00082 | 0.465 |
CLV_PCSK_KEX2_1 | 259 | 261 | PF00082 | 0.345 |
CLV_PCSK_KEX2_1 | 428 | 430 | PF00082 | 0.466 |
CLV_PCSK_KEX2_1 | 545 | 547 | PF00082 | 0.317 |
CLV_PCSK_KEX2_1 | 574 | 576 | PF00082 | 0.767 |
CLV_PCSK_PC1ET2_1 | 574 | 576 | PF00082 | 0.601 |
CLV_PCSK_SKI1_1 | 194 | 198 | PF00082 | 0.390 |
CLV_PCSK_SKI1_1 | 228 | 232 | PF00082 | 0.500 |
CLV_PCSK_SKI1_1 | 445 | 449 | PF00082 | 0.394 |
CLV_PCSK_SKI1_1 | 545 | 549 | PF00082 | 0.291 |
CLV_PCSK_SKI1_1 | 70 | 74 | PF00082 | 0.463 |
DEG_APCC_DBOX_1 | 193 | 201 | PF00400 | 0.588 |
DEG_APCC_KENBOX_2 | 513 | 517 | PF00400 | 0.592 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.643 |
DOC_MAPK_gen_1 | 436 | 444 | PF00069 | 0.705 |
DOC_MAPK_gen_1 | 511 | 520 | PF00069 | 0.664 |
DOC_MAPK_gen_1 | 542 | 550 | PF00069 | 0.528 |
DOC_MAPK_MEF2A_6 | 404 | 413 | PF00069 | 0.520 |
DOC_MAPK_MEF2A_6 | 70 | 79 | PF00069 | 0.696 |
DOC_MAPK_RevD_3 | 184 | 199 | PF00069 | 0.544 |
DOC_PP1_RVXF_1 | 544 | 551 | PF00149 | 0.429 |
DOC_PP1_RVXF_1 | 74 | 80 | PF00149 | 0.634 |
DOC_USP7_MATH_1 | 119 | 123 | PF00917 | 0.764 |
DOC_USP7_MATH_1 | 132 | 136 | PF00917 | 0.710 |
DOC_USP7_MATH_1 | 248 | 252 | PF00917 | 0.691 |
DOC_USP7_MATH_1 | 275 | 279 | PF00917 | 0.652 |
DOC_USP7_MATH_1 | 286 | 290 | PF00917 | 0.680 |
DOC_USP7_MATH_1 | 430 | 434 | PF00917 | 0.521 |
DOC_USP7_MATH_1 | 451 | 455 | PF00917 | 0.617 |
DOC_USP7_MATH_1 | 541 | 545 | PF00917 | 0.701 |
DOC_USP7_MATH_2 | 275 | 281 | PF00917 | 0.617 |
DOC_WW_Pin1_4 | 519 | 524 | PF00397 | 0.631 |
LIG_14-3-3_CanoR_1 | 165 | 172 | PF00244 | 0.641 |
LIG_14-3-3_CanoR_1 | 208 | 212 | PF00244 | 0.553 |
LIG_14-3-3_CanoR_1 | 285 | 291 | PF00244 | 0.773 |
LIG_14-3-3_CanoR_1 | 41 | 51 | PF00244 | 0.678 |
LIG_14-3-3_CanoR_1 | 429 | 437 | PF00244 | 0.629 |
LIG_14-3-3_CanoR_1 | 490 | 494 | PF00244 | 0.610 |
LIG_14-3-3_CanoR_1 | 545 | 551 | PF00244 | 0.429 |
LIG_14-3-3_CanoR_1 | 6 | 12 | PF00244 | 0.634 |
LIG_Actin_WH2_2 | 65 | 80 | PF00022 | 0.699 |
LIG_Clathr_ClatBox_1 | 322 | 326 | PF01394 | 0.793 |
LIG_deltaCOP1_diTrp_1 | 500 | 509 | PF00928 | 0.563 |
LIG_eIF4E_1 | 172 | 178 | PF01652 | 0.543 |
LIG_FHA_1 | 307 | 313 | PF00498 | 0.740 |
LIG_FHA_1 | 418 | 424 | PF00498 | 0.639 |
LIG_FHA_1 | 46 | 52 | PF00498 | 0.608 |
LIG_FHA_1 | 565 | 571 | PF00498 | 0.550 |
LIG_FHA_2 | 64 | 70 | PF00498 | 0.689 |
LIG_LIR_Gen_1 | 210 | 218 | PF02991 | 0.697 |
LIG_LIR_Gen_1 | 7 | 14 | PF02991 | 0.552 |
LIG_LIR_Nem_3 | 210 | 214 | PF02991 | 0.695 |
LIG_LIR_Nem_3 | 308 | 314 | PF02991 | 0.634 |
LIG_LIR_Nem_3 | 549 | 553 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 55 | 61 | PF02991 | 0.580 |
LIG_LIR_Nem_3 | 7 | 11 | PF02991 | 0.655 |
LIG_PDZ_Class_3 | 575 | 580 | PF00595 | 0.520 |
LIG_SH2_NCK_1 | 172 | 176 | PF00017 | 0.641 |
LIG_SH2_PTP2 | 561 | 564 | PF00017 | 0.255 |
LIG_SH2_SRC | 172 | 175 | PF00017 | 0.642 |
LIG_SH2_STAP1 | 211 | 215 | PF00017 | 0.622 |
LIG_SH2_STAT5 | 141 | 144 | PF00017 | 0.601 |
LIG_SH2_STAT5 | 311 | 314 | PF00017 | 0.686 |
LIG_SH2_STAT5 | 561 | 564 | PF00017 | 0.349 |
LIG_SH3_3 | 110 | 116 | PF00018 | 0.785 |
LIG_SH3_3 | 465 | 471 | PF00018 | 0.718 |
LIG_SH3_3 | 475 | 481 | PF00018 | 0.736 |
LIG_SUMO_SIM_anti_2 | 552 | 558 | PF11976 | 0.255 |
LIG_SUMO_SIM_par_1 | 10 | 19 | PF11976 | 0.703 |
LIG_SUMO_SIM_par_1 | 321 | 328 | PF11976 | 0.728 |
LIG_TYR_ITIM | 559 | 564 | PF00017 | 0.255 |
LIG_WRC_WIRS_1 | 211 | 216 | PF05994 | 0.526 |
LIG_WRC_WIRS_1 | 5 | 10 | PF05994 | 0.673 |
LIG_WRC_WIRS_1 | 547 | 552 | PF05994 | 0.255 |
MOD_CK1_1 | 114 | 120 | PF00069 | 0.666 |
MOD_CK1_1 | 122 | 128 | PF00069 | 0.649 |
MOD_CK1_1 | 210 | 216 | PF00069 | 0.601 |
MOD_CK1_1 | 26 | 32 | PF00069 | 0.680 |
MOD_CK1_1 | 45 | 51 | PF00069 | 0.705 |
MOD_CK1_1 | 454 | 460 | PF00069 | 0.738 |
MOD_CK1_1 | 569 | 575 | PF00069 | 0.373 |
MOD_CK2_1 | 141 | 147 | PF00069 | 0.599 |
MOD_CK2_1 | 210 | 216 | PF00069 | 0.621 |
MOD_CK2_1 | 248 | 254 | PF00069 | 0.679 |
MOD_CK2_1 | 54 | 60 | PF00069 | 0.647 |
MOD_CK2_1 | 63 | 69 | PF00069 | 0.637 |
MOD_CMANNOS | 499 | 502 | PF00535 | 0.436 |
MOD_CMANNOS | 510 | 513 | PF00535 | 0.437 |
MOD_GlcNHglycan | 250 | 253 | PF01048 | 0.523 |
MOD_GlcNHglycan | 254 | 257 | PF01048 | 0.493 |
MOD_GlcNHglycan | 293 | 296 | PF01048 | 0.600 |
MOD_GlcNHglycan | 363 | 367 | PF01048 | 0.501 |
MOD_GlcNHglycan | 451 | 454 | PF01048 | 0.487 |
MOD_GlcNHglycan | 458 | 461 | PF01048 | 0.467 |
MOD_GlcNHglycan | 463 | 467 | PF01048 | 0.445 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.707 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.750 |
MOD_GSK3_1 | 137 | 144 | PF00069 | 0.671 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.709 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.678 |
MOD_GSK3_1 | 244 | 251 | PF00069 | 0.676 |
MOD_GSK3_1 | 291 | 298 | PF00069 | 0.807 |
MOD_GSK3_1 | 321 | 328 | PF00069 | 0.717 |
MOD_GSK3_1 | 331 | 338 | PF00069 | 0.649 |
MOD_GSK3_1 | 358 | 365 | PF00069 | 0.717 |
MOD_GSK3_1 | 447 | 454 | PF00069 | 0.663 |
MOD_GSK3_1 | 566 | 573 | PF00069 | 0.426 |
MOD_N-GLC_1 | 306 | 311 | PF02516 | 0.477 |
MOD_N-GLC_1 | 495 | 500 | PF02516 | 0.434 |
MOD_N-GLC_1 | 526 | 531 | PF02516 | 0.506 |
MOD_NEK2_1 | 120 | 125 | PF00069 | 0.742 |
MOD_NEK2_1 | 137 | 142 | PF00069 | 0.514 |
MOD_NEK2_1 | 325 | 330 | PF00069 | 0.631 |
MOD_NEK2_1 | 4 | 9 | PF00069 | 0.668 |
MOD_NEK2_1 | 566 | 571 | PF00069 | 0.578 |
MOD_NEK2_2 | 141 | 146 | PF00069 | 0.625 |
MOD_PIKK_1 | 23 | 29 | PF00454 | 0.744 |
MOD_PIKK_1 | 295 | 301 | PF00454 | 0.812 |
MOD_PIKK_1 | 335 | 341 | PF00454 | 0.641 |
MOD_PIKK_1 | 45 | 51 | PF00454 | 0.634 |
MOD_PIKK_1 | 451 | 457 | PF00454 | 0.585 |
MOD_PKA_2 | 207 | 213 | PF00069 | 0.561 |
MOD_PKA_2 | 248 | 254 | PF00069 | 0.544 |
MOD_PKA_2 | 284 | 290 | PF00069 | 0.772 |
MOD_PKA_2 | 358 | 364 | PF00069 | 0.638 |
MOD_PKA_2 | 489 | 495 | PF00069 | 0.609 |
MOD_PKA_2 | 541 | 547 | PF00069 | 0.705 |
MOD_PKA_2 | 570 | 576 | PF00069 | 0.380 |
MOD_PKB_1 | 163 | 171 | PF00069 | 0.551 |
MOD_Plk_1 | 132 | 138 | PF00069 | 0.681 |
MOD_Plk_1 | 161 | 167 | PF00069 | 0.664 |
MOD_Plk_1 | 306 | 312 | PF00069 | 0.641 |
MOD_Plk_1 | 495 | 501 | PF00069 | 0.722 |
MOD_Plk_1 | 54 | 60 | PF00069 | 0.690 |
MOD_Plk_1 | 63 | 69 | PF00069 | 0.674 |
MOD_Plk_1 | 70 | 76 | PF00069 | 0.645 |
MOD_Plk_2-3 | 207 | 213 | PF00069 | 0.540 |
MOD_Plk_2-3 | 277 | 283 | PF00069 | 0.622 |
MOD_Plk_2-3 | 64 | 70 | PF00069 | 0.707 |
MOD_Plk_4 | 132 | 138 | PF00069 | 0.734 |
MOD_Plk_4 | 210 | 216 | PF00069 | 0.643 |
MOD_Plk_4 | 307 | 313 | PF00069 | 0.636 |
MOD_Plk_4 | 549 | 555 | PF00069 | 0.418 |
MOD_Plk_4 | 7 | 13 | PF00069 | 0.665 |
MOD_ProDKin_1 | 519 | 525 | PF00069 | 0.630 |
MOD_SUMO_for_1 | 236 | 239 | PF00179 | 0.656 |
MOD_SUMO_rev_2 | 433 | 437 | PF00179 | 0.634 |
TRG_DiLeu_BaEn_1 | 173 | 178 | PF01217 | 0.542 |
TRG_DiLeu_BaEn_1 | 227 | 232 | PF01217 | 0.664 |
TRG_DiLeu_BaEn_4 | 161 | 167 | PF01217 | 0.689 |
TRG_DiLeu_BaLyEn_6 | 543 | 548 | PF01217 | 0.576 |
TRG_ENDOCYTIC_2 | 211 | 214 | PF00928 | 0.656 |
TRG_ENDOCYTIC_2 | 561 | 564 | PF00928 | 0.464 |
TRG_ENDOCYTIC_2 | 58 | 61 | PF00928 | 0.664 |
TRG_ER_diArg_1 | 163 | 166 | PF00400 | 0.559 |
TRG_ER_diArg_1 | 258 | 260 | PF00400 | 0.669 |
TRG_ER_diArg_1 | 391 | 394 | PF00400 | 0.530 |
TRG_ER_diArg_1 | 476 | 479 | PF00400 | 0.604 |
TRG_ER_diArg_1 | 545 | 547 | PF00400 | 0.531 |
TRG_ER_diArg_1 | 75 | 78 | PF00400 | 0.621 |
TRG_NES_CRM1_1 | 42 | 55 | PF08389 | 0.537 |
TRG_Pf-PMV_PEXEL_1 | 198 | 203 | PF00026 | 0.431 |
TRG_Pf-PMV_PEXEL_1 | 259 | 263 | PF00026 | 0.470 |
TRG_Pf-PMV_PEXEL_1 | 379 | 383 | PF00026 | 0.498 |
TRG_Pf-PMV_PEXEL_1 | 59 | 63 | PF00026 | 0.463 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I4B6 | Leptomonas seymouri | 37% | 99% |
A0A1X0NV17 | Trypanosomatidae | 27% | 100% |
A0A3S7X5F4 | Leishmania donovani | 63% | 100% |
A4I7S1 | Leishmania infantum | 63% | 93% |
E9B2M9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 62% | 82% |
Q4Q5H8 | Leishmania major | 59% | 100% |
V5BGM1 | Trypanosoma cruzi | 27% | 100% |