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: A0A3Q8IDU7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 418 | 422 | PF00656 | 0.633 |
CLV_NRD_NRD_1 | 121 | 123 | PF00675 | 0.728 |
CLV_NRD_NRD_1 | 370 | 372 | PF00675 | 0.662 |
CLV_NRD_NRD_1 | 42 | 44 | PF00675 | 0.709 |
CLV_NRD_NRD_1 | 97 | 99 | PF00675 | 0.708 |
CLV_PCSK_FUR_1 | 40 | 44 | PF00082 | 0.707 |
CLV_PCSK_KEX2_1 | 121 | 123 | PF00082 | 0.723 |
CLV_PCSK_KEX2_1 | 343 | 345 | PF00082 | 0.720 |
CLV_PCSK_KEX2_1 | 370 | 372 | PF00082 | 0.662 |
CLV_PCSK_KEX2_1 | 42 | 44 | PF00082 | 0.709 |
CLV_PCSK_KEX2_1 | 97 | 99 | PF00082 | 0.708 |
CLV_PCSK_PC1ET2_1 | 343 | 345 | PF00082 | 0.720 |
DEG_SPOP_SBC_1 | 348 | 352 | PF00917 | 0.746 |
DOC_ANK_TNKS_1 | 451 | 458 | PF00023 | 0.748 |
DOC_CYCLIN_yCln2_LP_2 | 146 | 152 | PF00134 | 0.810 |
DOC_CYCLIN_yCln2_LP_2 | 273 | 279 | PF00134 | 0.615 |
DOC_PP2B_LxvP_1 | 189 | 192 | PF13499 | 0.670 |
DOC_PP2B_LxvP_1 | 273 | 276 | PF13499 | 0.507 |
DOC_PP4_FxxP_1 | 150 | 153 | PF00568 | 0.812 |
DOC_SPAK_OSR1_1 | 238 | 242 | PF12202 | 0.713 |
DOC_USP7_MATH_1 | 161 | 165 | PF00917 | 0.844 |
DOC_USP7_MATH_1 | 198 | 202 | PF00917 | 0.727 |
DOC_USP7_MATH_1 | 223 | 227 | PF00917 | 0.550 |
DOC_USP7_MATH_1 | 348 | 352 | PF00917 | 0.746 |
DOC_USP7_MATH_1 | 438 | 442 | PF00917 | 0.800 |
DOC_USP7_MATH_1 | 66 | 70 | PF00917 | 0.749 |
DOC_WW_Pin1_4 | 127 | 132 | PF00397 | 0.727 |
DOC_WW_Pin1_4 | 165 | 170 | PF00397 | 0.732 |
DOC_WW_Pin1_4 | 172 | 177 | PF00397 | 0.684 |
DOC_WW_Pin1_4 | 255 | 260 | PF00397 | 0.604 |
DOC_WW_Pin1_4 | 41 | 46 | PF00397 | 0.747 |
DOC_WW_Pin1_4 | 434 | 439 | PF00397 | 0.836 |
DOC_WW_Pin1_4 | 6 | 11 | PF00397 | 0.804 |
LIG_14-3-3_CanoR_1 | 238 | 242 | PF00244 | 0.588 |
LIG_14-3-3_CanoR_1 | 370 | 377 | PF00244 | 0.677 |
LIG_14-3-3_CanoR_1 | 394 | 402 | PF00244 | 0.595 |
LIG_14-3-3_CanoR_1 | 439 | 447 | PF00244 | 0.633 |
LIG_14-3-3_CanoR_1 | 64 | 74 | PF00244 | 0.727 |
LIG_14-3-3_CanoR_1 | 97 | 107 | PF00244 | 0.688 |
LIG_APCC_ABBA_1 | 241 | 246 | PF00400 | 0.465 |
LIG_APCC_ABBA_1 | 90 | 95 | PF00400 | 0.764 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.810 |
LIG_BIR_III_4 | 421 | 425 | PF00653 | 0.717 |
LIG_BIR_III_4 | 429 | 433 | PF00653 | 0.629 |
LIG_BIR_III_4 | 480 | 484 | PF00653 | 0.738 |
LIG_deltaCOP1_diTrp_1 | 310 | 315 | PF00928 | 0.692 |
LIG_deltaCOP1_diTrp_1 | 373 | 380 | PF00928 | 0.608 |
LIG_FHA_1 | 166 | 172 | PF00498 | 0.771 |
LIG_FHA_1 | 34 | 40 | PF00498 | 0.762 |
LIG_FHA_1 | 370 | 376 | PF00498 | 0.689 |
LIG_FHA_1 | 386 | 392 | PF00498 | 0.579 |
LIG_FHA_1 | 397 | 403 | PF00498 | 0.616 |
LIG_FHA_1 | 42 | 48 | PF00498 | 0.721 |
LIG_FHA_1 | 448 | 454 | PF00498 | 0.677 |
LIG_FHA_2 | 410 | 416 | PF00498 | 0.741 |
LIG_LIR_Gen_1 | 132 | 142 | PF02991 | 0.664 |
LIG_LIR_Gen_1 | 521 | 530 | PF02991 | 0.755 |
LIG_LIR_Nem_3 | 13 | 18 | PF02991 | 0.783 |
LIG_LIR_Nem_3 | 132 | 137 | PF02991 | 0.744 |
LIG_LIR_Nem_3 | 140 | 145 | PF02991 | 0.647 |
LIG_LIR_Nem_3 | 374 | 380 | PF02991 | 0.602 |
LIG_LIR_Nem_3 | 521 | 526 | PF02991 | 0.758 |
LIG_LIR_Nem_3 | 91 | 96 | PF02991 | 0.695 |
LIG_PCNA_PIPBox_1 | 498 | 507 | PF02747 | 0.692 |
LIG_SH2_CRK | 134 | 138 | PF00017 | 0.745 |
LIG_SH2_PTP2 | 270 | 273 | PF00017 | 0.547 |
LIG_SH2_STAP1 | 134 | 138 | PF00017 | 0.745 |
LIG_SH2_STAT3 | 282 | 285 | PF00017 | 0.615 |
LIG_SH2_STAT3 | 324 | 327 | PF00017 | 0.626 |
LIG_SH2_STAT5 | 181 | 184 | PF00017 | 0.608 |
LIG_SH2_STAT5 | 270 | 273 | PF00017 | 0.569 |
LIG_SH2_STAT5 | 33 | 36 | PF00017 | 0.730 |
LIG_SH3_3 | 101 | 107 | PF00018 | 0.616 |
LIG_SH3_3 | 146 | 152 | PF00018 | 0.743 |
LIG_SH3_3 | 166 | 172 | PF00018 | 0.576 |
LIG_SH3_3 | 295 | 301 | PF00018 | 0.680 |
LIG_SH3_3 | 441 | 447 | PF00018 | 0.751 |
LIG_SH3_3 | 514 | 520 | PF00018 | 0.689 |
LIG_SUMO_SIM_anti_2 | 78 | 84 | PF11976 | 0.649 |
LIG_TRAF2_1 | 416 | 419 | PF00917 | 0.626 |
LIG_UBA3_1 | 379 | 387 | PF00899 | 0.644 |
MOD_CDK_SPK_2 | 41 | 46 | PF00069 | 0.747 |
MOD_CDK_SPK_2 | 434 | 439 | PF00069 | 0.622 |
MOD_CK1_1 | 126 | 132 | PF00069 | 0.803 |
MOD_CK1_1 | 365 | 371 | PF00069 | 0.708 |
MOD_CK1_1 | 413 | 419 | PF00069 | 0.813 |
MOD_CK1_1 | 437 | 443 | PF00069 | 0.747 |
MOD_CK1_1 | 53 | 59 | PF00069 | 0.829 |
MOD_CK1_1 | 68 | 74 | PF00069 | 0.572 |
MOD_CK2_1 | 334 | 340 | PF00069 | 0.742 |
MOD_CK2_1 | 349 | 355 | PF00069 | 0.808 |
MOD_CK2_1 | 409 | 415 | PF00069 | 0.729 |
MOD_Cter_Amidation | 119 | 122 | PF01082 | 0.611 |
MOD_GlcNHglycan | 202 | 205 | PF01048 | 0.678 |
MOD_GlcNHglycan | 218 | 222 | PF01048 | 0.562 |
MOD_GlcNHglycan | 252 | 255 | PF01048 | 0.605 |
MOD_GlcNHglycan | 29 | 32 | PF01048 | 0.681 |
MOD_GlcNHglycan | 328 | 331 | PF01048 | 0.552 |
MOD_GlcNHglycan | 351 | 354 | PF01048 | 0.739 |
MOD_GlcNHglycan | 412 | 415 | PF01048 | 0.834 |
MOD_GlcNHglycan | 52 | 55 | PF01048 | 0.808 |
MOD_GlcNHglycan | 70 | 73 | PF01048 | 0.534 |
MOD_GlcNHglycan | 86 | 90 | PF01048 | 0.501 |
MOD_GSK3_1 | 122 | 129 | PF00069 | 0.822 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.660 |
MOD_GSK3_1 | 223 | 230 | PF00069 | 0.586 |
MOD_GSK3_1 | 334 | 341 | PF00069 | 0.753 |
MOD_GSK3_1 | 343 | 350 | PF00069 | 0.625 |
MOD_GSK3_1 | 365 | 372 | PF00069 | 0.723 |
MOD_GSK3_1 | 405 | 412 | PF00069 | 0.684 |
MOD_GSK3_1 | 41 | 48 | PF00069 | 0.784 |
MOD_GSK3_1 | 434 | 441 | PF00069 | 0.814 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.708 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.745 |
MOD_N-GLC_1 | 405 | 410 | PF02516 | 0.759 |
MOD_N-GLC_1 | 66 | 71 | PF02516 | 0.747 |
MOD_NEK2_1 | 113 | 118 | PF00069 | 0.754 |
MOD_NEK2_1 | 137 | 142 | PF00069 | 0.678 |
MOD_NEK2_1 | 217 | 222 | PF00069 | 0.679 |
MOD_NEK2_1 | 326 | 331 | PF00069 | 0.730 |
MOD_NEK2_1 | 349 | 354 | PF00069 | 0.696 |
MOD_NEK2_1 | 380 | 385 | PF00069 | 0.719 |
MOD_NEK2_2 | 59 | 64 | PF00069 | 0.614 |
MOD_PIKK_1 | 114 | 120 | PF00454 | 0.749 |
MOD_PIKK_1 | 33 | 39 | PF00454 | 0.697 |
MOD_PIKK_1 | 405 | 411 | PF00454 | 0.802 |
MOD_PK_1 | 280 | 286 | PF00069 | 0.726 |
MOD_PKA_1 | 343 | 349 | PF00069 | 0.728 |
MOD_PKA_2 | 237 | 243 | PF00069 | 0.625 |
MOD_PKA_2 | 333 | 339 | PF00069 | 0.714 |
MOD_PKA_2 | 343 | 349 | PF00069 | 0.672 |
MOD_PKA_2 | 369 | 375 | PF00069 | 0.727 |
MOD_PKA_2 | 438 | 444 | PF00069 | 0.678 |
MOD_PKA_2 | 45 | 51 | PF00069 | 0.811 |
MOD_Plk_1 | 280 | 286 | PF00069 | 0.698 |
MOD_Plk_1 | 334 | 340 | PF00069 | 0.786 |
MOD_Plk_1 | 85 | 91 | PF00069 | 0.742 |
MOD_Plk_2-3 | 369 | 375 | PF00069 | 0.649 |
MOD_Plk_4 | 380 | 386 | PF00069 | 0.719 |
MOD_Plk_4 | 387 | 393 | PF00069 | 0.566 |
MOD_Plk_4 | 440 | 446 | PF00069 | 0.713 |
MOD_ProDKin_1 | 127 | 133 | PF00069 | 0.725 |
MOD_ProDKin_1 | 165 | 171 | PF00069 | 0.730 |
MOD_ProDKin_1 | 172 | 178 | PF00069 | 0.676 |
MOD_ProDKin_1 | 255 | 261 | PF00069 | 0.604 |
MOD_ProDKin_1 | 41 | 47 | PF00069 | 0.749 |
MOD_ProDKin_1 | 434 | 440 | PF00069 | 0.837 |
MOD_ProDKin_1 | 6 | 12 | PF00069 | 0.804 |
TRG_DiLeu_BaLyEn_6 | 173 | 178 | PF01217 | 0.751 |
TRG_ENDOCYTIC_2 | 134 | 137 | PF00928 | 0.721 |
TRG_ENDOCYTIC_2 | 270 | 273 | PF00928 | 0.569 |
TRG_ENDOCYTIC_2 | 523 | 526 | PF00928 | 0.645 |
TRG_ENDOCYTIC_2 | 93 | 96 | PF00928 | 0.677 |
TRG_ER_diArg_1 | 121 | 123 | PF00400 | 0.725 |
TRG_ER_diArg_1 | 41 | 43 | PF00400 | 0.709 |
TRG_ER_diArg_1 | 96 | 98 | PF00400 | 0.697 |
TRG_NES_CRM1_1 | 456 | 469 | PF08389 | 0.629 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HXW3 | Leptomonas seymouri | 26% | 92% |
A4HHJ8 | Leishmania braziliensis | 68% | 100% |
A4I4Q7 | Leishmania infantum | 99% | 100% |
E9AE60 | Leishmania major | 88% | 100% |
E9ALM5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |