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: A0A3Q8IBX4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 459 | 463 | PF00656 | 0.686 |
CLV_NRD_NRD_1 | 117 | 119 | PF00675 | 0.625 |
CLV_NRD_NRD_1 | 148 | 150 | PF00675 | 0.632 |
CLV_NRD_NRD_1 | 387 | 389 | PF00675 | 0.683 |
CLV_NRD_NRD_1 | 434 | 436 | PF00675 | 0.622 |
CLV_NRD_NRD_1 | 453 | 455 | PF00675 | 0.474 |
CLV_NRD_NRD_1 | 480 | 482 | PF00675 | 0.581 |
CLV_NRD_NRD_1 | 9 | 11 | PF00675 | 0.720 |
CLV_PCSK_KEX2_1 | 116 | 118 | PF00082 | 0.573 |
CLV_PCSK_KEX2_1 | 148 | 150 | PF00082 | 0.632 |
CLV_PCSK_KEX2_1 | 387 | 389 | PF00082 | 0.683 |
CLV_PCSK_KEX2_1 | 453 | 455 | PF00082 | 0.678 |
CLV_PCSK_KEX2_1 | 517 | 519 | PF00082 | 0.659 |
CLV_PCSK_PC1ET2_1 | 116 | 118 | PF00082 | 0.585 |
CLV_PCSK_PC1ET2_1 | 517 | 519 | PF00082 | 0.659 |
CLV_PCSK_PC7_1 | 112 | 118 | PF00082 | 0.676 |
CLV_PCSK_SKI1_1 | 117 | 121 | PF00082 | 0.677 |
CLV_PCSK_SKI1_1 | 413 | 417 | PF00082 | 0.664 |
CLV_PCSK_SKI1_1 | 436 | 440 | PF00082 | 0.634 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.677 |
DEG_SCF_FBW7_1 | 313 | 319 | PF00400 | 0.726 |
DEG_SPOP_SBC_1 | 71 | 75 | PF00917 | 0.808 |
DOC_CKS1_1 | 313 | 318 | PF01111 | 0.725 |
DOC_CYCLIN_yCln2_LP_2 | 20 | 26 | PF00134 | 0.769 |
DOC_MAPK_gen_1 | 517 | 523 | PF00069 | 0.682 |
DOC_MAPK_RevD_3 | 440 | 454 | PF00069 | 0.683 |
DOC_PP2B_LxvP_1 | 20 | 23 | PF13499 | 0.807 |
DOC_PP2B_LxvP_1 | 442 | 445 | PF13499 | 0.689 |
DOC_PP4_FxxP_1 | 297 | 300 | PF00568 | 0.798 |
DOC_PP4_FxxP_1 | 371 | 374 | PF00568 | 0.777 |
DOC_PP4_MxPP_1 | 438 | 441 | PF00568 | 0.674 |
DOC_USP7_MATH_1 | 265 | 269 | PF00917 | 0.634 |
DOC_USP7_MATH_1 | 290 | 294 | PF00917 | 0.793 |
DOC_USP7_MATH_1 | 334 | 338 | PF00917 | 0.732 |
DOC_USP7_MATH_1 | 72 | 76 | PF00917 | 0.769 |
DOC_WW_Pin1_4 | 296 | 301 | PF00397 | 0.780 |
DOC_WW_Pin1_4 | 312 | 317 | PF00397 | 0.821 |
DOC_WW_Pin1_4 | 320 | 325 | PF00397 | 0.749 |
DOC_WW_Pin1_4 | 404 | 409 | PF00397 | 0.680 |
LIG_14-3-3_CanoR_1 | 256 | 260 | PF00244 | 0.709 |
LIG_14-3-3_CanoR_1 | 289 | 295 | PF00244 | 0.625 |
LIG_14-3-3_CanoR_1 | 435 | 439 | PF00244 | 0.610 |
LIG_Actin_WH2_2 | 85 | 101 | PF00022 | 0.695 |
LIG_BRCT_BRCA1_1 | 336 | 340 | PF00533 | 0.726 |
LIG_EVH1_1 | 41 | 45 | PF00568 | 0.616 |
LIG_EVH1_1 | 439 | 443 | PF00568 | 0.676 |
LIG_FHA_1 | 171 | 177 | PF00498 | 0.531 |
LIG_FHA_1 | 289 | 295 | PF00498 | 0.663 |
LIG_FHA_1 | 396 | 402 | PF00498 | 0.625 |
LIG_FHA_1 | 414 | 420 | PF00498 | 0.604 |
LIG_FHA_1 | 71 | 77 | PF00498 | 0.811 |
LIG_FHA_2 | 139 | 145 | PF00498 | 0.611 |
LIG_FHA_2 | 237 | 243 | PF00498 | 0.653 |
LIG_FHA_2 | 348 | 354 | PF00498 | 0.816 |
LIG_FHA_2 | 472 | 478 | PF00498 | 0.601 |
LIG_LIR_Apic_2 | 369 | 374 | PF02991 | 0.672 |
LIG_LIR_Gen_1 | 251 | 261 | PF02991 | 0.607 |
LIG_LIR_Nem_3 | 251 | 257 | PF02991 | 0.610 |
LIG_MYND_1 | 440 | 444 | PF01753 | 0.689 |
LIG_PDZ_Class_2 | 518 | 523 | PF00595 | 0.680 |
LIG_PDZ_Wminus1_1 | 521 | 523 | PF00595 | 0.756 |
LIG_PTAP_UEV_1 | 302 | 307 | PF05743 | 0.714 |
LIG_PTB_Apo_2 | 56 | 63 | PF02174 | 0.809 |
LIG_SH2_CRK | 364 | 368 | PF00017 | 0.736 |
LIG_SH2_CRK | 491 | 495 | PF00017 | 0.650 |
LIG_SH2_CRK | 95 | 99 | PF00017 | 0.667 |
LIG_SH2_NCK_1 | 429 | 433 | PF00017 | 0.724 |
LIG_SH2_PTP2 | 254 | 257 | PF00017 | 0.612 |
LIG_SH2_STAP1 | 2 | 6 | PF00017 | 0.679 |
LIG_SH2_STAP1 | 429 | 433 | PF00017 | 0.627 |
LIG_SH2_STAT3 | 188 | 191 | PF00017 | 0.544 |
LIG_SH2_STAT5 | 188 | 191 | PF00017 | 0.576 |
LIG_SH2_STAT5 | 254 | 257 | PF00017 | 0.612 |
LIG_SH2_STAT5 | 364 | 367 | PF00017 | 0.655 |
LIG_SH2_STAT5 | 370 | 373 | PF00017 | 0.663 |
LIG_SH2_STAT5 | 488 | 491 | PF00017 | 0.629 |
LIG_SH3_2 | 441 | 446 | PF14604 | 0.764 |
LIG_SH3_3 | 297 | 303 | PF00018 | 0.728 |
LIG_SH3_3 | 310 | 316 | PF00018 | 0.637 |
LIG_SH3_3 | 333 | 339 | PF00018 | 0.693 |
LIG_SH3_3 | 380 | 386 | PF00018 | 0.735 |
LIG_SH3_3 | 39 | 45 | PF00018 | 0.660 |
LIG_SH3_3 | 402 | 408 | PF00018 | 0.707 |
LIG_SH3_3 | 437 | 443 | PF00018 | 0.756 |
LIG_SH3_3 | 506 | 512 | PF00018 | 0.775 |
LIG_SH3_3 | 76 | 82 | PF00018 | 0.793 |
LIG_SH3_CIN85_PxpxPR_1 | 441 | 446 | PF14604 | 0.764 |
LIG_TRAF2_1 | 136 | 139 | PF00917 | 0.688 |
LIG_TRAF2_1 | 200 | 203 | PF00917 | 0.518 |
LIG_TRAF2_1 | 249 | 252 | PF00917 | 0.632 |
LIG_TRAF2_1 | 350 | 353 | PF00917 | 0.599 |
LIG_TYR_ITIM | 362 | 367 | PF00017 | 0.692 |
LIG_TYR_ITIM | 489 | 494 | PF00017 | 0.640 |
LIG_WRC_WIRS_1 | 1 | 6 | PF05994 | 0.668 |
LIG_WW_2 | 440 | 443 | PF00397 | 0.686 |
LIG_WW_3 | 443 | 447 | PF00397 | 0.765 |
MOD_CK1_1 | 12 | 18 | PF00069 | 0.692 |
MOD_CK1_1 | 207 | 213 | PF00069 | 0.667 |
MOD_CK1_1 | 220 | 226 | PF00069 | 0.733 |
MOD_CK1_1 | 235 | 241 | PF00069 | 0.664 |
MOD_CK1_1 | 299 | 305 | PF00069 | 0.769 |
MOD_CK1_1 | 5 | 11 | PF00069 | 0.786 |
MOD_CK2_1 | 138 | 144 | PF00069 | 0.564 |
MOD_CK2_1 | 347 | 353 | PF00069 | 0.785 |
MOD_Cter_Amidation | 515 | 518 | PF01082 | 0.663 |
MOD_GlcNHglycan | 11 | 14 | PF01048 | 0.693 |
MOD_GlcNHglycan | 17 | 20 | PF01048 | 0.691 |
MOD_GlcNHglycan | 234 | 237 | PF01048 | 0.713 |
MOD_GlcNHglycan | 303 | 306 | PF01048 | 0.719 |
MOD_GlcNHglycan | 336 | 339 | PF01048 | 0.746 |
MOD_GlcNHglycan | 374 | 377 | PF01048 | 0.766 |
MOD_GlcNHglycan | 429 | 432 | PF01048 | 0.622 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.751 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.782 |
MOD_GSK3_1 | 304 | 311 | PF00069 | 0.810 |
MOD_GSK3_1 | 312 | 319 | PF00069 | 0.707 |
MOD_GSK3_1 | 320 | 327 | PF00069 | 0.735 |
MOD_GSK3_1 | 372 | 379 | PF00069 | 0.658 |
MOD_GSK3_1 | 409 | 416 | PF00069 | 0.651 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.669 |
MOD_N-GLC_1 | 15 | 20 | PF02516 | 0.699 |
MOD_N-GLC_1 | 497 | 502 | PF02516 | 0.720 |
MOD_NEK2_1 | 204 | 209 | PF00069 | 0.700 |
MOD_NEK2_1 | 460 | 465 | PF00069 | 0.589 |
MOD_NEK2_1 | 489 | 494 | PF00069 | 0.640 |
MOD_NEK2_2 | 72 | 77 | PF00069 | 0.812 |
MOD_PIKK_1 | 170 | 176 | PF00454 | 0.532 |
MOD_PIKK_1 | 304 | 310 | PF00454 | 0.836 |
MOD_PKA_2 | 170 | 176 | PF00069 | 0.532 |
MOD_PKA_2 | 189 | 195 | PF00069 | 0.555 |
MOD_PKA_2 | 255 | 261 | PF00069 | 0.708 |
MOD_PKA_2 | 288 | 294 | PF00069 | 0.681 |
MOD_PKA_2 | 434 | 440 | PF00069 | 0.722 |
MOD_PKA_2 | 460 | 466 | PF00069 | 0.686 |
MOD_PKA_2 | 9 | 15 | PF00069 | 0.626 |
MOD_Plk_1 | 102 | 108 | PF00069 | 0.521 |
MOD_Plk_1 | 446 | 452 | PF00069 | 0.753 |
MOD_Plk_2-3 | 471 | 477 | PF00069 | 0.630 |
MOD_Plk_4 | 184 | 190 | PF00069 | 0.557 |
MOD_Plk_4 | 362 | 368 | PF00069 | 0.612 |
MOD_Plk_4 | 434 | 440 | PF00069 | 0.722 |
MOD_Plk_4 | 460 | 466 | PF00069 | 0.585 |
MOD_Plk_4 | 72 | 78 | PF00069 | 0.811 |
MOD_ProDKin_1 | 296 | 302 | PF00069 | 0.779 |
MOD_ProDKin_1 | 312 | 318 | PF00069 | 0.823 |
MOD_ProDKin_1 | 320 | 326 | PF00069 | 0.747 |
MOD_ProDKin_1 | 404 | 410 | PF00069 | 0.678 |
MOD_SUMO_for_1 | 126 | 129 | PF00179 | 0.579 |
MOD_SUMO_rev_2 | 33 | 37 | PF00179 | 0.783 |
MOD_SUMO_rev_2 | 477 | 484 | PF00179 | 0.696 |
TRG_ENDOCYTIC_2 | 254 | 257 | PF00928 | 0.612 |
TRG_ENDOCYTIC_2 | 364 | 367 | PF00928 | 0.738 |
TRG_ENDOCYTIC_2 | 491 | 494 | PF00928 | 0.650 |
TRG_ENDOCYTIC_2 | 95 | 98 | PF00928 | 0.618 |
TRG_ER_diArg_1 | 148 | 150 | PF00400 | 0.637 |
TRG_ER_diArg_1 | 285 | 288 | PF00400 | 0.773 |
TRG_ER_diArg_1 | 386 | 388 | PF00400 | 0.683 |
TRG_ER_diArg_1 | 452 | 454 | PF00400 | 0.690 |
TRG_NLS_MonoCore_2 | 114 | 119 | PF00514 | 0.598 |
TRG_NLS_MonoExtN_4 | 112 | 119 | PF00514 | 0.633 |
TRG_Pf-PMV_PEXEL_1 | 118 | 122 | PF00026 | 0.575 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7J5 | Leptomonas seymouri | 45% | 100% |
A4H5N6 | Leishmania braziliensis | 74% | 100% |
A4HU08 | Leishmania infantum | 100% | 100% |
E9AMT8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 99% |
Q4QHT7 | Leishmania major | 92% | 100% |