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: Q4QEB7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 42 | 44 | PF00675 | 0.507 |
CLV_NRD_NRD_1 | 437 | 439 | PF00675 | 0.591 |
CLV_NRD_NRD_1 | 85 | 87 | PF00675 | 0.435 |
CLV_PCSK_KEX2_1 | 42 | 44 | PF00082 | 0.510 |
CLV_PCSK_KEX2_1 | 437 | 439 | PF00082 | 0.591 |
CLV_PCSK_SKI1_1 | 61 | 65 | PF00082 | 0.524 |
CLV_PCSK_SKI1_1 | 93 | 97 | PF00082 | 0.494 |
DEG_APCC_DBOX_1 | 42 | 50 | PF00400 | 0.502 |
DEG_SCF_FBW7_1 | 344 | 351 | PF00400 | 0.648 |
DEG_SPOP_SBC_1 | 310 | 314 | PF00917 | 0.618 |
DEG_SPOP_SBC_1 | 462 | 466 | PF00917 | 0.698 |
DOC_CDC14_PxL_1 | 337 | 345 | PF14671 | 0.682 |
DOC_CKS1_1 | 220 | 225 | PF01111 | 0.688 |
DOC_CKS1_1 | 255 | 260 | PF01111 | 0.729 |
DOC_CYCLIN_yCln2_LP_2 | 416 | 422 | PF00134 | 0.612 |
DOC_MAPK_gen_1 | 145 | 154 | PF00069 | 0.496 |
DOC_MAPK_MEF2A_6 | 145 | 154 | PF00069 | 0.496 |
DOC_PP1_RVXF_1 | 435 | 442 | PF00149 | 0.541 |
DOC_PP2B_LxvP_1 | 416 | 419 | PF13499 | 0.621 |
DOC_PP4_FxxP_1 | 20 | 23 | PF00568 | 0.456 |
DOC_USP7_MATH_1 | 105 | 109 | PF00917 | 0.603 |
DOC_USP7_MATH_1 | 128 | 132 | PF00917 | 0.511 |
DOC_USP7_MATH_1 | 16 | 20 | PF00917 | 0.504 |
DOC_USP7_MATH_1 | 205 | 209 | PF00917 | 0.680 |
DOC_USP7_MATH_1 | 210 | 214 | PF00917 | 0.821 |
DOC_USP7_MATH_1 | 276 | 280 | PF00917 | 0.666 |
DOC_USP7_MATH_1 | 305 | 309 | PF00917 | 0.664 |
DOC_USP7_MATH_1 | 310 | 314 | PF00917 | 0.587 |
DOC_USP7_MATH_1 | 318 | 322 | PF00917 | 0.646 |
DOC_USP7_MATH_1 | 331 | 335 | PF00917 | 0.727 |
DOC_USP7_MATH_1 | 348 | 352 | PF00917 | 0.534 |
DOC_USP7_MATH_1 | 359 | 363 | PF00917 | 0.565 |
DOC_USP7_MATH_1 | 370 | 374 | PF00917 | 0.773 |
DOC_USP7_MATH_1 | 375 | 379 | PF00917 | 0.632 |
DOC_USP7_MATH_1 | 391 | 395 | PF00917 | 0.676 |
DOC_USP7_MATH_1 | 485 | 489 | PF00917 | 0.762 |
DOC_USP7_MATH_1 | 97 | 101 | PF00917 | 0.595 |
DOC_USP7_UBL2_3 | 141 | 145 | PF12436 | 0.478 |
DOC_WW_Pin1_4 | 103 | 108 | PF00397 | 0.509 |
DOC_WW_Pin1_4 | 219 | 224 | PF00397 | 0.629 |
DOC_WW_Pin1_4 | 254 | 259 | PF00397 | 0.692 |
DOC_WW_Pin1_4 | 272 | 277 | PF00397 | 0.511 |
DOC_WW_Pin1_4 | 314 | 319 | PF00397 | 0.730 |
DOC_WW_Pin1_4 | 344 | 349 | PF00397 | 0.615 |
DOC_WW_Pin1_4 | 355 | 360 | PF00397 | 0.618 |
DOC_WW_Pin1_4 | 402 | 407 | PF00397 | 0.684 |
DOC_WW_Pin1_4 | 464 | 469 | PF00397 | 0.635 |
LIG_14-3-3_CanoR_1 | 162 | 168 | PF00244 | 0.570 |
LIG_14-3-3_CanoR_1 | 173 | 180 | PF00244 | 0.454 |
LIG_14-3-3_CanoR_1 | 240 | 248 | PF00244 | 0.680 |
LIG_14-3-3_CanoR_1 | 409 | 416 | PF00244 | 0.607 |
LIG_14-3-3_CanoR_1 | 93 | 102 | PF00244 | 0.559 |
LIG_Actin_WH2_2 | 290 | 305 | PF00022 | 0.443 |
LIG_BRCT_BRCA1_1 | 184 | 188 | PF00533 | 0.661 |
LIG_BRCT_BRCA1_1 | 487 | 491 | PF00533 | 0.638 |
LIG_EVH1_1 | 340 | 344 | PF00568 | 0.594 |
LIG_FHA_1 | 133 | 139 | PF00498 | 0.580 |
LIG_FHA_1 | 147 | 153 | PF00498 | 0.370 |
LIG_FHA_1 | 255 | 261 | PF00498 | 0.710 |
LIG_FHA_2 | 193 | 199 | PF00498 | 0.711 |
LIG_LIR_Apic_2 | 18 | 23 | PF02991 | 0.452 |
LIG_LIR_Gen_1 | 169 | 179 | PF02991 | 0.503 |
LIG_LIR_Gen_1 | 488 | 496 | PF02991 | 0.630 |
LIG_LIR_Nem_3 | 169 | 174 | PF02991 | 0.529 |
LIG_LIR_Nem_3 | 488 | 494 | PF02991 | 0.635 |
LIG_NRBOX | 34 | 40 | PF00104 | 0.434 |
LIG_NRBOX | 454 | 460 | PF00104 | 0.607 |
LIG_Pex14_2 | 20 | 24 | PF04695 | 0.494 |
LIG_PTB_Apo_2 | 73 | 80 | PF02174 | 0.437 |
LIG_PTB_Phospho_1 | 73 | 79 | PF10480 | 0.437 |
LIG_SH2_STAP1 | 235 | 239 | PF00017 | 0.631 |
LIG_SH2_STAT3 | 392 | 395 | PF00017 | 0.716 |
LIG_SH3_3 | 225 | 231 | PF00018 | 0.628 |
LIG_SH3_3 | 338 | 344 | PF00018 | 0.783 |
LIG_SUMO_SIM_anti_2 | 282 | 287 | PF11976 | 0.552 |
LIG_TRAF2_1 | 431 | 434 | PF00917 | 0.563 |
LIG_UBA3_1 | 38 | 45 | PF00899 | 0.420 |
LIG_WW_2 | 341 | 344 | PF00397 | 0.593 |
MOD_CDK_SPxK_1 | 344 | 350 | PF00069 | 0.618 |
MOD_CDK_SPxxK_3 | 402 | 409 | PF00069 | 0.685 |
MOD_CDK_SPxxK_3 | 464 | 471 | PF00069 | 0.542 |
MOD_CK1_1 | 106 | 112 | PF00069 | 0.570 |
MOD_CK1_1 | 308 | 314 | PF00069 | 0.573 |
MOD_CK1_1 | 317 | 323 | PF00069 | 0.646 |
MOD_CK1_1 | 360 | 366 | PF00069 | 0.688 |
MOD_CK1_1 | 461 | 467 | PF00069 | 0.644 |
MOD_CK1_1 | 475 | 481 | PF00069 | 0.714 |
MOD_CK1_1 | 492 | 498 | PF00069 | 0.495 |
MOD_CK2_1 | 192 | 198 | PF00069 | 0.681 |
MOD_CK2_1 | 276 | 282 | PF00069 | 0.561 |
MOD_CK2_1 | 322 | 328 | PF00069 | 0.642 |
MOD_GlcNHglycan | 111 | 114 | PF01048 | 0.592 |
MOD_GlcNHglycan | 163 | 166 | PF01048 | 0.548 |
MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.624 |
MOD_GlcNHglycan | 207 | 210 | PF01048 | 0.698 |
MOD_GlcNHglycan | 212 | 215 | PF01048 | 0.670 |
MOD_GlcNHglycan | 260 | 263 | PF01048 | 0.716 |
MOD_GlcNHglycan | 324 | 327 | PF01048 | 0.741 |
MOD_GlcNHglycan | 337 | 340 | PF01048 | 0.781 |
MOD_GlcNHglycan | 359 | 362 | PF01048 | 0.679 |
MOD_GlcNHglycan | 363 | 366 | PF01048 | 0.628 |
MOD_GlcNHglycan | 383 | 386 | PF01048 | 0.578 |
MOD_GlcNHglycan | 395 | 398 | PF01048 | 0.662 |
MOD_GlcNHglycan | 477 | 480 | PF01048 | 0.732 |
MOD_GlcNHglycan | 487 | 490 | PF01048 | 0.637 |
MOD_GlcNHglycan | 494 | 497 | PF01048 | 0.534 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.606 |
MOD_GSK3_1 | 124 | 131 | PF00069 | 0.569 |
MOD_GSK3_1 | 182 | 189 | PF00069 | 0.657 |
MOD_GSK3_1 | 254 | 261 | PF00069 | 0.813 |
MOD_GSK3_1 | 272 | 279 | PF00069 | 0.508 |
MOD_GSK3_1 | 305 | 312 | PF00069 | 0.550 |
MOD_GSK3_1 | 314 | 321 | PF00069 | 0.642 |
MOD_GSK3_1 | 331 | 338 | PF00069 | 0.774 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.630 |
MOD_GSK3_1 | 355 | 362 | PF00069 | 0.608 |
MOD_GSK3_1 | 458 | 465 | PF00069 | 0.558 |
MOD_GSK3_1 | 485 | 492 | PF00069 | 0.758 |
MOD_GSK3_1 | 93 | 100 | PF00069 | 0.453 |
MOD_N-GLC_1 | 182 | 187 | PF02516 | 0.599 |
MOD_NEK2_1 | 132 | 137 | PF00069 | 0.502 |
MOD_NEK2_1 | 309 | 314 | PF00069 | 0.588 |
MOD_NEK2_1 | 41 | 46 | PF00069 | 0.395 |
MOD_NEK2_1 | 451 | 456 | PF00069 | 0.545 |
MOD_NEK2_1 | 458 | 463 | PF00069 | 0.515 |
MOD_NEK2_2 | 97 | 102 | PF00069 | 0.454 |
MOD_PIKK_1 | 119 | 125 | PF00454 | 0.597 |
MOD_PIKK_1 | 132 | 138 | PF00454 | 0.434 |
MOD_PIKK_1 | 199 | 205 | PF00454 | 0.698 |
MOD_PIKK_1 | 391 | 397 | PF00454 | 0.667 |
MOD_PKA_2 | 146 | 152 | PF00069 | 0.459 |
MOD_PKA_2 | 161 | 167 | PF00069 | 0.402 |
MOD_PKA_2 | 205 | 211 | PF00069 | 0.717 |
MOD_PKA_2 | 239 | 245 | PF00069 | 0.626 |
MOD_PKA_2 | 408 | 414 | PF00069 | 0.609 |
MOD_PKA_2 | 41 | 47 | PF00069 | 0.395 |
MOD_PKA_2 | 472 | 478 | PF00069 | 0.719 |
MOD_Plk_1 | 31 | 37 | PF00069 | 0.517 |
MOD_Plk_1 | 411 | 417 | PF00069 | 0.691 |
MOD_Plk_2-3 | 472 | 478 | PF00069 | 0.669 |
MOD_Plk_4 | 31 | 37 | PF00069 | 0.574 |
MOD_ProDKin_1 | 103 | 109 | PF00069 | 0.515 |
MOD_ProDKin_1 | 219 | 225 | PF00069 | 0.629 |
MOD_ProDKin_1 | 254 | 260 | PF00069 | 0.694 |
MOD_ProDKin_1 | 272 | 278 | PF00069 | 0.505 |
MOD_ProDKin_1 | 314 | 320 | PF00069 | 0.733 |
MOD_ProDKin_1 | 344 | 350 | PF00069 | 0.618 |
MOD_ProDKin_1 | 355 | 361 | PF00069 | 0.618 |
MOD_ProDKin_1 | 402 | 408 | PF00069 | 0.683 |
MOD_ProDKin_1 | 464 | 470 | PF00069 | 0.637 |
MOD_SUMO_rev_2 | 11 | 19 | PF00179 | 0.368 |
TRG_DiLeu_BaLyEn_6 | 170 | 175 | PF01217 | 0.468 |
TRG_DiLeu_BaLyEn_6 | 297 | 302 | PF01217 | 0.508 |
TRG_ENDOCYTIC_2 | 235 | 238 | PF00928 | 0.634 |
TRG_ENDOCYTIC_2 | 85 | 88 | PF00928 | 0.356 |
TRG_ER_diArg_1 | 297 | 300 | PF00400 | 0.541 |
TRG_ER_diArg_1 | 41 | 43 | PF00400 | 0.501 |
TRG_ER_diArg_1 | 437 | 439 | PF00400 | 0.515 |
TRG_NES_CRM1_1 | 142 | 156 | PF08389 | 0.502 |
TRG_Pf-PMV_PEXEL_1 | 173 | 177 | PF00026 | 0.502 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PBW8 | Leptomonas seymouri | 40% | 96% |
A0A3S5H709 | Leishmania donovani | 93% | 100% |
A4H919 | Leishmania braziliensis | 70% | 96% |
A4HXF1 | Leishmania infantum | 93% | 100% |
E9AR46 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |