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: 11 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: A0A3Q8ICD1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 164 | 168 | PF00656 | 0.523 |
CLV_NRD_NRD_1 | 534 | 536 | PF00675 | 0.430 |
CLV_PCSK_SKI1_1 | 132 | 136 | PF00082 | 0.433 |
CLV_PCSK_SKI1_1 | 333 | 337 | PF00082 | 0.523 |
CLV_PCSK_SKI1_1 | 40 | 44 | PF00082 | 0.339 |
CLV_PCSK_SKI1_1 | 65 | 69 | PF00082 | 0.490 |
CLV_PCSK_SKI1_1 | 85 | 89 | PF00082 | 0.535 |
DEG_APCC_DBOX_1 | 458 | 466 | PF00400 | 0.572 |
DEG_APCC_DBOX_1 | 546 | 554 | PF00400 | 0.360 |
DOC_CYCLIN_yCln2_LP_2 | 433 | 439 | PF00134 | 0.560 |
DOC_MAPK_DCC_7 | 105 | 114 | PF00069 | 0.360 |
DOC_MAPK_FxFP_2 | 209 | 212 | PF00069 | 0.304 |
DOC_MAPK_gen_1 | 128 | 137 | PF00069 | 0.507 |
DOC_MAPK_gen_1 | 372 | 380 | PF00069 | 0.469 |
DOC_MAPK_HePTP_8 | 102 | 114 | PF00069 | 0.443 |
DOC_MAPK_MEF2A_6 | 105 | 114 | PF00069 | 0.590 |
DOC_MAPK_MEF2A_6 | 131 | 139 | PF00069 | 0.497 |
DOC_MAPK_MEF2A_6 | 284 | 292 | PF00069 | 0.371 |
DOC_MAPK_MEF2A_6 | 297 | 306 | PF00069 | 0.391 |
DOC_MAPK_MEF2A_6 | 381 | 389 | PF00069 | 0.562 |
DOC_MAPK_NFAT4_5 | 132 | 140 | PF00069 | 0.490 |
DOC_PP1_RVXF_1 | 266 | 272 | PF00149 | 0.357 |
DOC_PP1_RVXF_1 | 33 | 40 | PF00149 | 0.372 |
DOC_PP1_RVXF_1 | 83 | 89 | PF00149 | 0.530 |
DOC_PP4_FxxP_1 | 209 | 212 | PF00568 | 0.353 |
DOC_PP4_FxxP_1 | 88 | 91 | PF00568 | 0.615 |
DOC_USP7_MATH_1 | 11 | 15 | PF00917 | 0.662 |
DOC_USP7_MATH_1 | 245 | 249 | PF00917 | 0.489 |
DOC_USP7_MATH_1 | 311 | 315 | PF00917 | 0.446 |
DOC_USP7_MATH_1 | 455 | 459 | PF00917 | 0.661 |
DOC_USP7_MATH_1 | 47 | 51 | PF00917 | 0.481 |
DOC_USP7_MATH_1 | 5 | 9 | PF00917 | 0.718 |
DOC_USP7_MATH_1 | 522 | 526 | PF00917 | 0.420 |
DOC_USP7_MATH_1 | 91 | 95 | PF00917 | 0.636 |
DOC_USP7_UBL2_3 | 31 | 35 | PF12436 | 0.374 |
DOC_WW_Pin1_4 | 184 | 189 | PF00397 | 0.433 |
DOC_WW_Pin1_4 | 190 | 195 | PF00397 | 0.564 |
DOC_WW_Pin1_4 | 20 | 25 | PF00397 | 0.613 |
DOC_WW_Pin1_4 | 400 | 405 | PF00397 | 0.726 |
DOC_WW_Pin1_4 | 432 | 437 | PF00397 | 0.759 |
DOC_WW_Pin1_4 | 490 | 495 | PF00397 | 0.420 |
DOC_WW_Pin1_4 | 558 | 563 | PF00397 | 0.436 |
LIG_14-3-3_CanoR_1 | 203 | 208 | PF00244 | 0.298 |
LIG_14-3-3_CanoR_1 | 268 | 277 | PF00244 | 0.349 |
LIG_14-3-3_CanoR_1 | 406 | 410 | PF00244 | 0.530 |
LIG_14-3-3_CanoR_1 | 547 | 555 | PF00244 | 0.439 |
LIG_14-3-3_CanoR_1 | 575 | 584 | PF00244 | 0.420 |
LIG_Actin_WH2_2 | 115 | 130 | PF00022 | 0.397 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.649 |
LIG_BRCT_BRCA1_1 | 492 | 496 | PF00533 | 0.377 |
LIG_BRCT_BRCA1_1 | 541 | 545 | PF00533 | 0.464 |
LIG_BRCT_BRCA1_1 | 582 | 586 | PF00533 | 0.469 |
LIG_BRCT_BRCA1_1 | 71 | 75 | PF00533 | 0.532 |
LIG_Clathr_ClatBox_1 | 41 | 45 | PF01394 | 0.346 |
LIG_EH_1 | 453 | 457 | PF12763 | 0.669 |
LIG_FHA_1 | 154 | 160 | PF00498 | 0.495 |
LIG_FHA_1 | 199 | 205 | PF00498 | 0.429 |
LIG_FHA_1 | 272 | 278 | PF00498 | 0.334 |
LIG_FHA_1 | 31 | 37 | PF00498 | 0.371 |
LIG_FHA_1 | 325 | 331 | PF00498 | 0.356 |
LIG_FHA_1 | 471 | 477 | PF00498 | 0.405 |
LIG_FHA_1 | 487 | 493 | PF00498 | 0.584 |
LIG_FHA_1 | 589 | 595 | PF00498 | 0.412 |
LIG_FHA_2 | 162 | 168 | PF00498 | 0.411 |
LIG_FHA_2 | 191 | 197 | PF00498 | 0.496 |
LIG_FHA_2 | 44 | 50 | PF00498 | 0.416 |
LIG_FHA_2 | 499 | 505 | PF00498 | 0.385 |
LIG_LIR_Apic_2 | 206 | 212 | PF02991 | 0.354 |
LIG_LIR_Gen_1 | 149 | 160 | PF02991 | 0.317 |
LIG_LIR_Gen_1 | 234 | 244 | PF02991 | 0.388 |
LIG_LIR_Gen_1 | 542 | 553 | PF02991 | 0.415 |
LIG_LIR_Gen_1 | 593 | 603 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 149 | 155 | PF02991 | 0.506 |
LIG_LIR_Nem_3 | 189 | 195 | PF02991 | 0.454 |
LIG_LIR_Nem_3 | 196 | 202 | PF02991 | 0.336 |
LIG_LIR_Nem_3 | 208 | 214 | PF02991 | 0.322 |
LIG_LIR_Nem_3 | 234 | 239 | PF02991 | 0.492 |
LIG_LIR_Nem_3 | 32 | 37 | PF02991 | 0.373 |
LIG_LIR_Nem_3 | 542 | 548 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 583 | 589 | PF02991 | 0.388 |
LIG_LIR_Nem_3 | 590 | 595 | PF02991 | 0.389 |
LIG_LIR_Nem_3 | 98 | 102 | PF02991 | 0.542 |
LIG_Pex14_2 | 271 | 275 | PF04695 | 0.300 |
LIG_PTAP_UEV_1 | 297 | 302 | PF05743 | 0.404 |
LIG_SH2_CRK | 199 | 203 | PF00017 | 0.465 |
LIG_SH2_CRK | 351 | 355 | PF00017 | 0.565 |
LIG_SH2_CRK | 595 | 599 | PF00017 | 0.435 |
LIG_SH2_STAT5 | 152 | 155 | PF00017 | 0.374 |
LIG_SH2_STAT5 | 222 | 225 | PF00017 | 0.361 |
LIG_SH2_STAT5 | 252 | 255 | PF00017 | 0.348 |
LIG_SH2_STAT5 | 270 | 273 | PF00017 | 0.315 |
LIG_SH2_STAT5 | 577 | 580 | PF00017 | 0.479 |
LIG_SH2_STAT5 | 587 | 590 | PF00017 | 0.400 |
LIG_SH3_3 | 295 | 301 | PF00018 | 0.438 |
LIG_SH3_3 | 449 | 455 | PF00018 | 0.657 |
LIG_SUMO_SIM_anti_2 | 499 | 504 | PF11976 | 0.398 |
LIG_SUMO_SIM_par_1 | 115 | 123 | PF11976 | 0.371 |
LIG_SUMO_SIM_par_1 | 40 | 46 | PF11976 | 0.467 |
LIG_SUMO_SIM_par_1 | 566 | 572 | PF11976 | 0.436 |
LIG_TRAF2_1 | 337 | 340 | PF00917 | 0.549 |
LIG_UBA3_1 | 462 | 468 | PF00899 | 0.533 |
LIG_WRC_WIRS_1 | 211 | 216 | PF05994 | 0.349 |
MOD_CDC14_SPxK_1 | 403 | 406 | PF00782 | 0.703 |
MOD_CDK_SPxK_1 | 400 | 406 | PF00069 | 0.703 |
MOD_CK1_1 | 14 | 20 | PF00069 | 0.563 |
MOD_CK1_1 | 248 | 254 | PF00069 | 0.477 |
MOD_CK1_1 | 314 | 320 | PF00069 | 0.464 |
MOD_CK1_1 | 4 | 10 | PF00069 | 0.649 |
MOD_CK1_1 | 417 | 423 | PF00069 | 0.546 |
MOD_CK1_1 | 431 | 437 | PF00069 | 0.551 |
MOD_CK1_1 | 466 | 472 | PF00069 | 0.431 |
MOD_CK1_1 | 51 | 57 | PF00069 | 0.579 |
MOD_CK1_1 | 518 | 524 | PF00069 | 0.446 |
MOD_CK1_1 | 569 | 575 | PF00069 | 0.466 |
MOD_CK1_1 | 80 | 86 | PF00069 | 0.601 |
MOD_CK2_1 | 190 | 196 | PF00069 | 0.535 |
MOD_CK2_1 | 417 | 423 | PF00069 | 0.652 |
MOD_CK2_1 | 97 | 103 | PF00069 | 0.570 |
MOD_Cter_Amidation | 129 | 132 | PF01082 | 0.452 |
MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.525 |
MOD_GlcNHglycan | 247 | 250 | PF01048 | 0.483 |
MOD_GlcNHglycan | 271 | 274 | PF01048 | 0.393 |
MOD_GlcNHglycan | 298 | 301 | PF01048 | 0.400 |
MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.649 |
MOD_GlcNHglycan | 313 | 316 | PF01048 | 0.484 |
MOD_GlcNHglycan | 356 | 359 | PF01048 | 0.620 |
MOD_GlcNHglycan | 414 | 417 | PF01048 | 0.616 |
MOD_GlcNHglycan | 520 | 523 | PF01048 | 0.431 |
MOD_GlcNHglycan | 99 | 102 | PF01048 | 0.454 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.665 |
MOD_GSK3_1 | 14 | 21 | PF00069 | 0.539 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.533 |
MOD_GSK3_1 | 198 | 205 | PF00069 | 0.333 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.340 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.485 |
MOD_GSK3_1 | 248 | 255 | PF00069 | 0.444 |
MOD_GSK3_1 | 271 | 278 | PF00069 | 0.364 |
MOD_GSK3_1 | 292 | 299 | PF00069 | 0.426 |
MOD_GSK3_1 | 310 | 317 | PF00069 | 0.598 |
MOD_GSK3_1 | 324 | 331 | PF00069 | 0.317 |
MOD_GSK3_1 | 417 | 424 | PF00069 | 0.630 |
MOD_GSK3_1 | 428 | 435 | PF00069 | 0.483 |
MOD_GSK3_1 | 43 | 50 | PF00069 | 0.409 |
MOD_GSK3_1 | 466 | 473 | PF00069 | 0.400 |
MOD_GSK3_1 | 486 | 493 | PF00069 | 0.476 |
MOD_GSK3_1 | 518 | 525 | PF00069 | 0.410 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.657 |
MOD_N-GLC_1 | 190 | 195 | PF02516 | 0.570 |
MOD_N-GLC_1 | 231 | 236 | PF02516 | 0.334 |
MOD_N-GLC_1 | 275 | 280 | PF02516 | 0.503 |
MOD_N-GLC_1 | 292 | 297 | PF02516 | 0.428 |
MOD_N-GLC_1 | 325 | 330 | PF02516 | 0.388 |
MOD_N-GLC_1 | 360 | 365 | PF02516 | 0.590 |
MOD_N-GLC_1 | 441 | 446 | PF02516 | 0.599 |
MOD_N-GLC_1 | 463 | 468 | PF02516 | 0.472 |
MOD_N-GLC_1 | 548 | 553 | PF02516 | 0.417 |
MOD_N-GLC_1 | 598 | 603 | PF02516 | 0.552 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.614 |
MOD_NEK2_1 | 146 | 151 | PF00069 | 0.382 |
MOD_NEK2_1 | 18 | 23 | PF00069 | 0.449 |
MOD_NEK2_1 | 214 | 219 | PF00069 | 0.402 |
MOD_NEK2_1 | 271 | 276 | PF00069 | 0.327 |
MOD_NEK2_1 | 392 | 397 | PF00069 | 0.596 |
MOD_NEK2_1 | 463 | 468 | PF00069 | 0.480 |
MOD_NEK2_1 | 496 | 501 | PF00069 | 0.328 |
MOD_NEK2_1 | 598 | 603 | PF00069 | 0.477 |
MOD_NEK2_1 | 67 | 72 | PF00069 | 0.405 |
MOD_NEK2_2 | 30 | 35 | PF00069 | 0.334 |
MOD_NEK2_2 | 522 | 527 | PF00069 | 0.449 |
MOD_PIKK_1 | 139 | 145 | PF00454 | 0.557 |
MOD_PIKK_1 | 255 | 261 | PF00454 | 0.457 |
MOD_PIKK_1 | 292 | 298 | PF00454 | 0.420 |
MOD_PIKK_1 | 335 | 341 | PF00454 | 0.424 |
MOD_PIKK_1 | 463 | 469 | PF00454 | 0.467 |
MOD_PIKK_1 | 48 | 54 | PF00454 | 0.535 |
MOD_PIKK_1 | 539 | 545 | PF00454 | 0.515 |
MOD_PIKK_1 | 575 | 581 | PF00454 | 0.434 |
MOD_PIKK_1 | 80 | 86 | PF00454 | 0.402 |
MOD_PIKK_1 | 91 | 97 | PF00454 | 0.522 |
MOD_PKA_2 | 104 | 110 | PF00069 | 0.501 |
MOD_PKA_2 | 202 | 208 | PF00069 | 0.296 |
MOD_PKA_2 | 405 | 411 | PF00069 | 0.587 |
MOD_PKA_2 | 447 | 453 | PF00069 | 0.651 |
MOD_Plk_1 | 234 | 240 | PF00069 | 0.359 |
MOD_Plk_1 | 325 | 331 | PF00069 | 0.392 |
MOD_Plk_1 | 441 | 447 | PF00069 | 0.569 |
MOD_Plk_1 | 48 | 54 | PF00069 | 0.409 |
MOD_Plk_1 | 598 | 604 | PF00069 | 0.558 |
MOD_Plk_2-3 | 590 | 596 | PF00069 | 0.416 |
MOD_Plk_4 | 141 | 147 | PF00069 | 0.459 |
MOD_Plk_4 | 179 | 185 | PF00069 | 0.446 |
MOD_Plk_4 | 210 | 216 | PF00069 | 0.368 |
MOD_Plk_4 | 248 | 254 | PF00069 | 0.492 |
MOD_Plk_4 | 441 | 447 | PF00069 | 0.576 |
MOD_Plk_4 | 498 | 504 | PF00069 | 0.489 |
MOD_Plk_4 | 590 | 596 | PF00069 | 0.431 |
MOD_Plk_4 | 599 | 605 | PF00069 | 0.463 |
MOD_ProDKin_1 | 184 | 190 | PF00069 | 0.439 |
MOD_ProDKin_1 | 20 | 26 | PF00069 | 0.609 |
MOD_ProDKin_1 | 400 | 406 | PF00069 | 0.727 |
MOD_ProDKin_1 | 432 | 438 | PF00069 | 0.757 |
MOD_ProDKin_1 | 490 | 496 | PF00069 | 0.410 |
MOD_ProDKin_1 | 558 | 564 | PF00069 | 0.430 |
TRG_DiLeu_BaEn_1 | 32 | 37 | PF01217 | 0.400 |
TRG_DiLeu_BaLyEn_6 | 339 | 344 | PF01217 | 0.450 |
TRG_DiLeu_BaLyEn_6 | 458 | 463 | PF01217 | 0.602 |
TRG_ENDOCYTIC_2 | 152 | 155 | PF00928 | 0.410 |
TRG_ENDOCYTIC_2 | 199 | 202 | PF00928 | 0.463 |
TRG_ENDOCYTIC_2 | 211 | 214 | PF00928 | 0.466 |
TRG_ENDOCYTIC_2 | 351 | 354 | PF00928 | 0.593 |
TRG_ENDOCYTIC_2 | 595 | 598 | PF00928 | 0.423 |
TRG_ER_diArg_1 | 553 | 556 | PF00400 | 0.455 |
TRG_ER_FFAT_2 | 514 | 525 | PF00635 | 0.530 |
TRG_NES_CRM1_1 | 221 | 235 | PF08389 | 0.401 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HRF1 | Leptomonas seymouri | 78% | 100% |
A0A0S4J7N2 | Bodo saltans | 29% | 74% |
A0A1X0NTT4 | Trypanosomatidae | 52% | 100% |
A0A3R7K4C8 | Trypanosoma rangeli | 54% | 100% |
A4HCJ4 | Leishmania braziliensis | 88% | 100% |
A4I014 | Leishmania infantum | 100% | 100% |
C9ZQ83 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% |
E9AVY7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 97% | 100% |
Q4QBJ2 | Leishmania major | 96% | 100% |
V5BGJ4 | Trypanosoma cruzi | 53% | 100% |