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 | yes | yes: 2, no: 4 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: A0A3Q8I7H5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 241 | 245 | PF00656 | 0.452 |
CLV_NRD_NRD_1 | 159 | 161 | PF00675 | 0.790 |
CLV_NRD_NRD_1 | 170 | 172 | PF00675 | 0.528 |
CLV_NRD_NRD_1 | 178 | 180 | PF00675 | 0.366 |
CLV_NRD_NRD_1 | 247 | 249 | PF00675 | 0.557 |
CLV_NRD_NRD_1 | 363 | 365 | PF00675 | 0.674 |
CLV_NRD_NRD_1 | 427 | 429 | PF00675 | 0.777 |
CLV_NRD_NRD_1 | 441 | 443 | PF00675 | 0.694 |
CLV_NRD_NRD_1 | 472 | 474 | PF00675 | 0.714 |
CLV_PCSK_KEX2_1 | 159 | 161 | PF00082 | 0.790 |
CLV_PCSK_KEX2_1 | 170 | 172 | PF00082 | 0.528 |
CLV_PCSK_KEX2_1 | 178 | 180 | PF00082 | 0.366 |
CLV_PCSK_KEX2_1 | 247 | 249 | PF00082 | 0.560 |
CLV_PCSK_KEX2_1 | 340 | 342 | PF00082 | 0.574 |
CLV_PCSK_KEX2_1 | 363 | 365 | PF00082 | 0.643 |
CLV_PCSK_KEX2_1 | 374 | 376 | PF00082 | 0.618 |
CLV_PCSK_KEX2_1 | 427 | 429 | PF00082 | 0.603 |
CLV_PCSK_KEX2_1 | 479 | 481 | PF00082 | 0.639 |
CLV_PCSK_KEX2_1 | 485 | 487 | PF00082 | 0.595 |
CLV_PCSK_PC1ET2_1 | 340 | 342 | PF00082 | 0.591 |
CLV_PCSK_PC1ET2_1 | 374 | 376 | PF00082 | 0.636 |
CLV_PCSK_PC1ET2_1 | 479 | 481 | PF00082 | 0.639 |
CLV_PCSK_PC1ET2_1 | 485 | 487 | PF00082 | 0.595 |
CLV_PCSK_SKI1_1 | 3 | 7 | PF00082 | 0.540 |
CLV_PCSK_SKI1_1 | 442 | 446 | PF00082 | 0.691 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.557 |
DEG_SPOP_SBC_1 | 142 | 146 | PF00917 | 0.541 |
DEG_SPOP_SBC_1 | 451 | 455 | PF00917 | 0.574 |
DOC_CYCLIN_yCln2_LP_2 | 297 | 303 | PF00134 | 0.643 |
DOC_PP2B_LxvP_1 | 297 | 300 | PF13499 | 0.641 |
DOC_USP7_MATH_1 | 123 | 127 | PF00917 | 0.712 |
DOC_USP7_MATH_1 | 142 | 146 | PF00917 | 0.754 |
DOC_USP7_MATH_1 | 271 | 275 | PF00917 | 0.604 |
DOC_USP7_MATH_1 | 368 | 372 | PF00917 | 0.712 |
DOC_USP7_MATH_1 | 39 | 43 | PF00917 | 0.694 |
DOC_USP7_MATH_1 | 468 | 472 | PF00917 | 0.777 |
DOC_USP7_UBL2_3 | 320 | 324 | PF12436 | 0.614 |
DOC_USP7_UBL2_3 | 397 | 401 | PF12436 | 0.647 |
DOC_USP7_UBL2_3 | 430 | 434 | PF12436 | 0.623 |
DOC_USP7_UBL2_3 | 439 | 443 | PF12436 | 0.641 |
DOC_USP7_UBL2_3 | 446 | 450 | PF12436 | 0.594 |
DOC_USP7_UBL2_3 | 474 | 478 | PF12436 | 0.633 |
DOC_WW_Pin1_4 | 195 | 200 | PF00397 | 0.492 |
DOC_WW_Pin1_4 | 354 | 359 | PF00397 | 0.602 |
DOC_WW_Pin1_4 | 411 | 416 | PF00397 | 0.627 |
DOC_WW_Pin1_4 | 466 | 471 | PF00397 | 0.572 |
LIG_14-3-3_CanoR_1 | 236 | 243 | PF00244 | 0.412 |
LIG_14-3-3_CanoR_1 | 327 | 335 | PF00244 | 0.672 |
LIG_14-3-3_CanoR_1 | 409 | 415 | PF00244 | 0.551 |
LIG_14-3-3_CanoR_1 | 452 | 460 | PF00244 | 0.703 |
LIG_14-3-3_CanoR_1 | 473 | 481 | PF00244 | 0.640 |
LIG_Clathr_ClatBox_1 | 82 | 86 | PF01394 | 0.630 |
LIG_FHA_1 | 199 | 205 | PF00498 | 0.471 |
LIG_FHA_2 | 236 | 242 | PF00498 | 0.517 |
LIG_FHA_2 | 288 | 294 | PF00498 | 0.649 |
LIG_FHA_2 | 72 | 78 | PF00498 | 0.548 |
LIG_LIR_Nem_3 | 93 | 99 | PF02991 | 0.594 |
LIG_NRP_CendR_1 | 489 | 490 | PF00754 | 0.693 |
LIG_Pex14_2 | 100 | 104 | PF04695 | 0.531 |
LIG_Pex14_2 | 16 | 20 | PF04695 | 0.600 |
LIG_RPA_C_Fungi | 423 | 435 | PF08784 | 0.572 |
LIG_SH2_STAT5 | 96 | 99 | PF00017 | 0.582 |
LIG_SH3_1 | 401 | 407 | PF00018 | 0.611 |
LIG_SH3_2 | 404 | 409 | PF14604 | 0.613 |
LIG_SH3_3 | 193 | 199 | PF00018 | 0.502 |
LIG_SH3_3 | 362 | 368 | PF00018 | 0.735 |
LIG_SH3_3 | 401 | 407 | PF00018 | 0.574 |
LIG_SH3_3 | 445 | 451 | PF00018 | 0.663 |
LIG_SH3_4 | 439 | 446 | PF00018 | 0.706 |
LIG_SUMO_SIM_anti_2 | 111 | 118 | PF11976 | 0.603 |
LIG_SUMO_SIM_par_1 | 81 | 88 | PF11976 | 0.626 |
LIG_WRC_WIRS_1 | 17 | 22 | PF05994 | 0.503 |
MOD_CDK_SPK_2 | 354 | 359 | PF00069 | 0.650 |
MOD_CDK_SPxxK_3 | 466 | 473 | PF00069 | 0.573 |
MOD_CK1_1 | 143 | 149 | PF00069 | 0.758 |
MOD_CK1_1 | 18 | 24 | PF00069 | 0.570 |
MOD_CK1_1 | 184 | 190 | PF00069 | 0.590 |
MOD_CK1_1 | 195 | 201 | PF00069 | 0.532 |
MOD_CK1_1 | 276 | 282 | PF00069 | 0.732 |
MOD_CK1_1 | 31 | 37 | PF00069 | 0.686 |
MOD_CK1_1 | 357 | 363 | PF00069 | 0.579 |
MOD_CK2_1 | 141 | 147 | PF00069 | 0.543 |
MOD_CK2_1 | 235 | 241 | PF00069 | 0.441 |
MOD_CK2_1 | 287 | 293 | PF00069 | 0.654 |
MOD_GlcNHglycan | 117 | 120 | PF01048 | 0.644 |
MOD_GlcNHglycan | 183 | 186 | PF01048 | 0.598 |
MOD_GlcNHglycan | 21 | 24 | PF01048 | 0.641 |
MOD_GlcNHglycan | 278 | 281 | PF01048 | 0.773 |
MOD_GlcNHglycan | 30 | 33 | PF01048 | 0.678 |
MOD_GlcNHglycan | 324 | 327 | PF01048 | 0.663 |
MOD_GlcNHglycan | 336 | 339 | PF01048 | 0.585 |
MOD_GlcNHglycan | 41 | 44 | PF01048 | 0.452 |
MOD_GlcNHglycan | 470 | 473 | PF01048 | 0.604 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.557 |
MOD_GSK3_1 | 141 | 148 | PF00069 | 0.623 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.602 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.519 |
MOD_GSK3_1 | 322 | 329 | PF00069 | 0.668 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.641 |
MOD_GSK3_1 | 370 | 377 | PF00069 | 0.779 |
MOD_GSK3_1 | 438 | 445 | PF00069 | 0.627 |
MOD_GSK3_1 | 446 | 453 | PF00069 | 0.689 |
MOD_GSK3_1 | 468 | 475 | PF00069 | 0.584 |
MOD_GSK3_1 | 67 | 74 | PF00069 | 0.605 |
MOD_N-GLC_1 | 219 | 224 | PF02516 | 0.433 |
MOD_N-GLC_1 | 354 | 359 | PF02516 | 0.638 |
MOD_N-GLC_1 | 88 | 93 | PF02516 | 0.594 |
MOD_NEK2_1 | 16 | 21 | PF00069 | 0.674 |
MOD_NEK2_1 | 203 | 208 | PF00069 | 0.477 |
MOD_NEK2_1 | 219 | 224 | PF00069 | 0.433 |
MOD_NEK2_1 | 410 | 415 | PF00069 | 0.549 |
MOD_NEK2_1 | 49 | 54 | PF00069 | 0.629 |
MOD_NEK2_2 | 58 | 63 | PF00069 | 0.766 |
MOD_PIKK_1 | 184 | 190 | PF00454 | 0.484 |
MOD_PIKK_1 | 203 | 209 | PF00454 | 0.625 |
MOD_PIKK_1 | 265 | 271 | PF00454 | 0.609 |
MOD_PIKK_1 | 273 | 279 | PF00454 | 0.585 |
MOD_PIKK_1 | 49 | 55 | PF00454 | 0.650 |
MOD_PIKK_1 | 61 | 67 | PF00454 | 0.524 |
MOD_PK_1 | 456 | 462 | PF00069 | 0.672 |
MOD_PKA_1 | 374 | 380 | PF00069 | 0.657 |
MOD_PKA_1 | 442 | 448 | PF00069 | 0.699 |
MOD_PKA_1 | 479 | 485 | PF00069 | 0.583 |
MOD_PKA_2 | 235 | 241 | PF00069 | 0.434 |
MOD_PKA_2 | 326 | 332 | PF00069 | 0.669 |
MOD_PKA_2 | 374 | 380 | PF00069 | 0.716 |
MOD_PKA_2 | 451 | 457 | PF00069 | 0.673 |
MOD_PKA_2 | 472 | 478 | PF00069 | 0.704 |
MOD_PKA_2 | 479 | 485 | PF00069 | 0.590 |
MOD_PKA_2 | 6 | 12 | PF00069 | 0.613 |
MOD_PKB_1 | 179 | 187 | PF00069 | 0.554 |
MOD_Plk_1 | 110 | 116 | PF00069 | 0.653 |
MOD_Plk_1 | 219 | 225 | PF00069 | 0.435 |
MOD_Plk_4 | 110 | 116 | PF00069 | 0.653 |
MOD_Plk_4 | 287 | 293 | PF00069 | 0.654 |
MOD_Plk_4 | 331 | 337 | PF00069 | 0.578 |
MOD_Plk_4 | 43 | 49 | PF00069 | 0.596 |
MOD_ProDKin_1 | 195 | 201 | PF00069 | 0.485 |
MOD_ProDKin_1 | 354 | 360 | PF00069 | 0.601 |
MOD_ProDKin_1 | 411 | 417 | PF00069 | 0.629 |
MOD_ProDKin_1 | 466 | 472 | PF00069 | 0.572 |
MOD_SUMO_for_1 | 226 | 229 | PF00179 | 0.435 |
TRG_ER_diArg_1 | 170 | 172 | PF00400 | 0.581 |
TRG_ER_diArg_1 | 178 | 181 | PF00400 | 0.433 |
TRG_ER_diArg_1 | 246 | 248 | PF00400 | 0.571 |
TRG_ER_diArg_1 | 341 | 344 | PF00400 | 0.688 |
TRG_ER_diArg_1 | 363 | 365 | PF00400 | 0.608 |
TRG_ER_diArg_1 | 460 | 463 | PF00400 | 0.608 |
TRG_NLS_MonoExtC_3 | 338 | 343 | PF00514 | 0.544 |
TRG_NLS_MonoExtN_4 | 339 | 344 | PF00514 | 0.533 |
TRG_Pf-PMV_PEXEL_1 | 107 | 111 | PF00026 | 0.580 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1ILW1 | Leptomonas seymouri | 44% | 95% |
A4H5N7 | Leishmania braziliensis | 65% | 100% |
A4HU09 | Leishmania infantum | 100% | 100% |
E9AMT9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 99% |
Q4QHT6 | Leishmania major | 89% | 99% |