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: E9AWW5
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 6 |
GO:0043167 | ion binding | 2 | 6 |
GO:0043169 | cation binding | 3 | 6 |
GO:0046872 | metal ion binding | 4 | 6 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 241 | 245 | PF00656 | 0.663 |
CLV_C14_Caspase3-7 | 437 | 441 | PF00656 | 0.287 |
CLV_NRD_NRD_1 | 102 | 104 | PF00675 | 0.616 |
CLV_NRD_NRD_1 | 225 | 227 | PF00675 | 0.375 |
CLV_NRD_NRD_1 | 364 | 366 | PF00675 | 0.444 |
CLV_NRD_NRD_1 | 508 | 510 | PF00675 | 0.460 |
CLV_NRD_NRD_1 | 577 | 579 | PF00675 | 0.430 |
CLV_PCSK_FUR_1 | 99 | 103 | PF00082 | 0.692 |
CLV_PCSK_KEX2_1 | 102 | 104 | PF00082 | 0.603 |
CLV_PCSK_KEX2_1 | 364 | 366 | PF00082 | 0.444 |
CLV_PCSK_KEX2_1 | 540 | 542 | PF00082 | 0.477 |
CLV_PCSK_KEX2_1 | 558 | 560 | PF00082 | 0.442 |
CLV_PCSK_KEX2_1 | 99 | 101 | PF00082 | 0.616 |
CLV_PCSK_PC1ET2_1 | 540 | 542 | PF00082 | 0.466 |
CLV_PCSK_PC1ET2_1 | 558 | 560 | PF00082 | 0.329 |
CLV_PCSK_SKI1_1 | 218 | 222 | PF00082 | 0.514 |
CLV_PCSK_SKI1_1 | 348 | 352 | PF00082 | 0.451 |
CLV_PCSK_SKI1_1 | 471 | 475 | PF00082 | 0.461 |
CLV_PCSK_SKI1_1 | 531 | 535 | PF00082 | 0.424 |
CLV_PCSK_SKI1_1 | 66 | 70 | PF00082 | 0.601 |
DEG_APCC_DBOX_1 | 217 | 225 | PF00400 | 0.338 |
DEG_APCC_DBOX_1 | 508 | 516 | PF00400 | 0.406 |
DEG_SPOP_SBC_1 | 318 | 322 | PF00917 | 0.706 |
DOC_CYCLIN_RxL_1 | 335 | 349 | PF00134 | 0.567 |
DOC_CYCLIN_RxL_1 | 466 | 477 | PF00134 | 0.509 |
DOC_CYCLIN_RxL_1 | 66 | 77 | PF00134 | 0.559 |
DOC_MAPK_gen_1 | 529 | 538 | PF00069 | 0.359 |
DOC_PP2B_LxvP_1 | 382 | 385 | PF13499 | 0.403 |
DOC_PP2B_LxvP_1 | 92 | 95 | PF13499 | 0.688 |
DOC_PP4_FxxP_1 | 139 | 142 | PF00568 | 0.497 |
DOC_PP4_FxxP_1 | 220 | 223 | PF00568 | 0.508 |
DOC_PP4_FxxP_1 | 253 | 256 | PF00568 | 0.660 |
DOC_USP7_MATH_1 | 109 | 113 | PF00917 | 0.646 |
DOC_USP7_MATH_1 | 130 | 134 | PF00917 | 0.714 |
DOC_USP7_MATH_1 | 154 | 158 | PF00917 | 0.742 |
DOC_USP7_MATH_1 | 235 | 239 | PF00917 | 0.632 |
DOC_USP7_MATH_1 | 242 | 246 | PF00917 | 0.640 |
DOC_USP7_MATH_1 | 247 | 251 | PF00917 | 0.604 |
DOC_USP7_MATH_1 | 309 | 313 | PF00917 | 0.769 |
DOC_USP7_MATH_1 | 331 | 335 | PF00917 | 0.645 |
DOC_USP7_MATH_1 | 34 | 38 | PF00917 | 0.572 |
DOC_USP7_MATH_1 | 434 | 438 | PF00917 | 0.344 |
DOC_USP7_MATH_1 | 554 | 558 | PF00917 | 0.404 |
DOC_USP7_MATH_1 | 75 | 79 | PF00917 | 0.530 |
DOC_USP7_MATH_2 | 34 | 40 | PF00917 | 0.513 |
DOC_WW_Pin1_4 | 112 | 117 | PF00397 | 0.623 |
DOC_WW_Pin1_4 | 138 | 143 | PF00397 | 0.722 |
DOC_WW_Pin1_4 | 156 | 161 | PF00397 | 0.558 |
DOC_WW_Pin1_4 | 181 | 186 | PF00397 | 0.488 |
DOC_WW_Pin1_4 | 227 | 232 | PF00397 | 0.683 |
DOC_WW_Pin1_4 | 251 | 256 | PF00397 | 0.716 |
DOC_WW_Pin1_4 | 277 | 282 | PF00397 | 0.584 |
DOC_WW_Pin1_4 | 314 | 319 | PF00397 | 0.550 |
DOC_WW_Pin1_4 | 351 | 356 | PF00397 | 0.584 |
DOC_WW_Pin1_4 | 408 | 413 | PF00397 | 0.332 |
DOC_WW_Pin1_4 | 477 | 482 | PF00397 | 0.486 |
DOC_WW_Pin1_4 | 550 | 555 | PF00397 | 0.414 |
DOC_WW_Pin1_4 | 615 | 620 | PF00397 | 0.581 |
LIG_14-3-3_CanoR_1 | 135 | 140 | PF00244 | 0.689 |
LIG_14-3-3_CanoR_1 | 175 | 185 | PF00244 | 0.377 |
LIG_14-3-3_CanoR_1 | 226 | 231 | PF00244 | 0.432 |
LIG_14-3-3_CanoR_1 | 442 | 447 | PF00244 | 0.431 |
LIG_14-3-3_CanoR_1 | 514 | 520 | PF00244 | 0.454 |
LIG_14-3-3_CanoR_1 | 581 | 589 | PF00244 | 0.464 |
LIG_14-3-3_CanoR_1 | 74 | 80 | PF00244 | 0.641 |
LIG_Actin_WH2_2 | 161 | 177 | PF00022 | 0.616 |
LIG_Actin_WH2_2 | 451 | 468 | PF00022 | 0.487 |
LIG_Actin_WH2_2 | 508 | 525 | PF00022 | 0.369 |
LIG_BIR_III_4 | 86 | 90 | PF00653 | 0.626 |
LIG_BRCT_BRCA1_1 | 249 | 253 | PF00533 | 0.536 |
LIG_BRCT_BRCA1_1 | 562 | 566 | PF00533 | 0.356 |
LIG_Clathr_ClatBox_1 | 516 | 520 | PF01394 | 0.331 |
LIG_FHA_1 | 266 | 272 | PF00498 | 0.579 |
LIG_FHA_1 | 280 | 286 | PF00498 | 0.588 |
LIG_FHA_1 | 309 | 315 | PF00498 | 0.661 |
LIG_FHA_1 | 39 | 45 | PF00498 | 0.559 |
LIG_FHA_1 | 516 | 522 | PF00498 | 0.411 |
LIG_FHA_1 | 53 | 59 | PF00498 | 0.624 |
LIG_FHA_1 | 67 | 73 | PF00498 | 0.548 |
LIG_FHA_1 | 74 | 80 | PF00498 | 0.561 |
LIG_FHA_2 | 186 | 192 | PF00498 | 0.397 |
LIG_FHA_2 | 239 | 245 | PF00498 | 0.665 |
LIG_FHA_2 | 386 | 392 | PF00498 | 0.522 |
LIG_FHA_2 | 575 | 581 | PF00498 | 0.466 |
LIG_LIR_Apic_2 | 137 | 142 | PF02991 | 0.495 |
LIG_LIR_Apic_2 | 250 | 256 | PF02991 | 0.528 |
LIG_LIR_Apic_2 | 550 | 554 | PF02991 | 0.387 |
LIG_LIR_Gen_1 | 207 | 213 | PF02991 | 0.484 |
LIG_LIR_Gen_1 | 494 | 502 | PF02991 | 0.364 |
LIG_LIR_Gen_1 | 563 | 573 | PF02991 | 0.363 |
LIG_LIR_Nem_3 | 207 | 211 | PF02991 | 0.485 |
LIG_LIR_Nem_3 | 327 | 333 | PF02991 | 0.703 |
LIG_LIR_Nem_3 | 411 | 417 | PF02991 | 0.427 |
LIG_LIR_Nem_3 | 453 | 458 | PF02991 | 0.502 |
LIG_LIR_Nem_3 | 494 | 498 | PF02991 | 0.356 |
LIG_LIR_Nem_3 | 562 | 567 | PF02991 | 0.364 |
LIG_LIR_Nem_3 | 568 | 573 | PF02991 | 0.365 |
LIG_LYPXL_yS_3 | 330 | 333 | PF13949 | 0.661 |
LIG_NRBOX | 511 | 517 | PF00104 | 0.372 |
LIG_PTB_Apo_2 | 592 | 599 | PF02174 | 0.354 |
LIG_SH2_CRK | 379 | 383 | PF00017 | 0.397 |
LIG_SH2_CRK | 455 | 459 | PF00017 | 0.495 |
LIG_SH2_CRK | 551 | 555 | PF00017 | 0.299 |
LIG_SH2_CRK | 573 | 577 | PF00017 | 0.444 |
LIG_SH2_NCK_1 | 305 | 309 | PF00017 | 0.574 |
LIG_SH2_NCK_1 | 573 | 577 | PF00017 | 0.444 |
LIG_SH2_SRC | 573 | 576 | PF00017 | 0.444 |
LIG_SH2_STAP1 | 305 | 309 | PF00017 | 0.574 |
LIG_SH2_STAT5 | 417 | 420 | PF00017 | 0.408 |
LIG_SH2_STAT5 | 429 | 432 | PF00017 | 0.384 |
LIG_SH3_3 | 113 | 119 | PF00018 | 0.644 |
LIG_SH3_3 | 157 | 163 | PF00018 | 0.685 |
LIG_SH3_3 | 249 | 255 | PF00018 | 0.656 |
LIG_SH3_3 | 312 | 318 | PF00018 | 0.711 |
LIG_SH3_3 | 334 | 340 | PF00018 | 0.677 |
LIG_SH3_3 | 352 | 358 | PF00018 | 0.596 |
LIG_SH3_3 | 409 | 415 | PF00018 | 0.318 |
LIG_SH3_3 | 419 | 425 | PF00018 | 0.289 |
LIG_SH3_3 | 57 | 63 | PF00018 | 0.595 |
LIG_TYR_ITIM | 206 | 211 | PF00017 | 0.475 |
LIG_TYR_ITIM | 377 | 382 | PF00017 | 0.378 |
LIG_UBA3_1 | 515 | 523 | PF00899 | 0.335 |
LIG_ULM_U2AF65_1 | 578 | 583 | PF00076 | 0.426 |
LIG_WRC_WIRS_1 | 136 | 141 | PF05994 | 0.501 |
LIG_WRC_WIRS_1 | 561 | 566 | PF05994 | 0.354 |
MOD_CDC14_SPxK_1 | 618 | 621 | PF00782 | 0.475 |
MOD_CDK_SPxK_1 | 615 | 621 | PF00069 | 0.453 |
MOD_CK1_1 | 112 | 118 | PF00069 | 0.598 |
MOD_CK1_1 | 137 | 143 | PF00069 | 0.689 |
MOD_CK1_1 | 156 | 162 | PF00069 | 0.786 |
MOD_CK1_1 | 238 | 244 | PF00069 | 0.671 |
MOD_CK1_1 | 245 | 251 | PF00069 | 0.826 |
MOD_CK1_1 | 266 | 272 | PF00069 | 0.686 |
MOD_CK1_1 | 300 | 306 | PF00069 | 0.614 |
MOD_CK1_1 | 317 | 323 | PF00069 | 0.599 |
MOD_CK1_1 | 325 | 331 | PF00069 | 0.727 |
MOD_CK1_1 | 39 | 45 | PF00069 | 0.756 |
MOD_CK1_1 | 477 | 483 | PF00069 | 0.545 |
MOD_CK1_1 | 49 | 55 | PF00069 | 0.531 |
MOD_CK2_1 | 181 | 187 | PF00069 | 0.484 |
MOD_CK2_1 | 267 | 273 | PF00069 | 0.695 |
MOD_CK2_1 | 385 | 391 | PF00069 | 0.523 |
MOD_CK2_1 | 544 | 550 | PF00069 | 0.459 |
MOD_CK2_1 | 574 | 580 | PF00069 | 0.458 |
MOD_Cter_Amidation | 97 | 100 | PF01082 | 0.695 |
MOD_DYRK1A_RPxSP_1 | 251 | 255 | PF00069 | 0.531 |
MOD_GlcNHglycan | 105 | 108 | PF01048 | 0.691 |
MOD_GlcNHglycan | 128 | 131 | PF01048 | 0.685 |
MOD_GlcNHglycan | 143 | 146 | PF01048 | 0.633 |
MOD_GlcNHglycan | 155 | 159 | PF01048 | 0.765 |
MOD_GlcNHglycan | 178 | 181 | PF01048 | 0.427 |
MOD_GlcNHglycan | 200 | 203 | PF01048 | 0.470 |
MOD_GlcNHglycan | 29 | 32 | PF01048 | 0.563 |
MOD_GlcNHglycan | 300 | 303 | PF01048 | 0.723 |
MOD_GlcNHglycan | 311 | 314 | PF01048 | 0.660 |
MOD_GlcNHglycan | 322 | 325 | PF01048 | 0.595 |
MOD_GlcNHglycan | 38 | 41 | PF01048 | 0.767 |
MOD_GlcNHglycan | 449 | 452 | PF01048 | 0.449 |
MOD_GlcNHglycan | 475 | 479 | PF01048 | 0.482 |
MOD_GlcNHglycan | 48 | 51 | PF01048 | 0.626 |
MOD_GlcNHglycan | 500 | 503 | PF01048 | 0.409 |
MOD_GlcNHglycan | 615 | 618 | PF01048 | 0.626 |
MOD_GlcNHglycan | 96 | 99 | PF01048 | 0.631 |
MOD_GSK3_1 | 122 | 129 | PF00069 | 0.643 |
MOD_GSK3_1 | 130 | 137 | PF00069 | 0.746 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.759 |
MOD_GSK3_1 | 181 | 188 | PF00069 | 0.460 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.551 |
MOD_GSK3_1 | 233 | 240 | PF00069 | 0.628 |
MOD_GSK3_1 | 247 | 254 | PF00069 | 0.605 |
MOD_GSK3_1 | 263 | 270 | PF00069 | 0.670 |
MOD_GSK3_1 | 294 | 301 | PF00069 | 0.648 |
MOD_GSK3_1 | 304 | 311 | PF00069 | 0.571 |
MOD_GSK3_1 | 314 | 321 | PF00069 | 0.559 |
MOD_GSK3_1 | 322 | 329 | PF00069 | 0.795 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.678 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.627 |
MOD_GSK3_1 | 442 | 449 | PF00069 | 0.419 |
MOD_GSK3_1 | 460 | 467 | PF00069 | 0.406 |
MOD_GSK3_1 | 496 | 503 | PF00069 | 0.362 |
MOD_GSK3_1 | 550 | 557 | PF00069 | 0.425 |
MOD_N-GLC_1 | 109 | 114 | PF02516 | 0.670 |
MOD_N-GLC_1 | 613 | 618 | PF02516 | 0.538 |
MOD_N-GLC_1 | 82 | 87 | PF02516 | 0.636 |
MOD_N-GLC_2 | 197 | 199 | PF02516 | 0.414 |
MOD_NEK2_1 | 126 | 131 | PF00069 | 0.752 |
MOD_NEK2_1 | 271 | 276 | PF00069 | 0.559 |
MOD_NEK2_1 | 446 | 451 | PF00069 | 0.342 |
MOD_NEK2_1 | 465 | 470 | PF00069 | 0.542 |
MOD_NEK2_1 | 500 | 505 | PF00069 | 0.408 |
MOD_NEK2_1 | 522 | 527 | PF00069 | 0.453 |
MOD_NEK2_1 | 560 | 565 | PF00069 | 0.359 |
MOD_NEK2_1 | 73 | 78 | PF00069 | 0.629 |
MOD_PIKK_1 | 162 | 168 | PF00454 | 0.580 |
MOD_PIKK_1 | 258 | 264 | PF00454 | 0.709 |
MOD_PIKK_1 | 434 | 440 | PF00454 | 0.461 |
MOD_PIKK_1 | 460 | 466 | PF00454 | 0.401 |
MOD_PK_1 | 263 | 269 | PF00069 | 0.628 |
MOD_PKA_1 | 101 | 107 | PF00069 | 0.695 |
MOD_PKA_1 | 226 | 232 | PF00069 | 0.439 |
MOD_PKA_2 | 101 | 107 | PF00069 | 0.683 |
MOD_PKA_2 | 134 | 140 | PF00069 | 0.689 |
MOD_PKA_2 | 21 | 27 | PF00069 | 0.615 |
MOD_PKA_2 | 225 | 231 | PF00069 | 0.415 |
MOD_PKA_2 | 580 | 586 | PF00069 | 0.438 |
MOD_PKA_2 | 73 | 79 | PF00069 | 0.748 |
MOD_PKB_1 | 99 | 107 | PF00069 | 0.696 |
MOD_Plk_1 | 109 | 115 | PF00069 | 0.658 |
MOD_Plk_1 | 406 | 412 | PF00069 | 0.442 |
MOD_Plk_4 | 185 | 191 | PF00069 | 0.421 |
MOD_Plk_4 | 442 | 448 | PF00069 | 0.337 |
MOD_Plk_4 | 75 | 81 | PF00069 | 0.563 |
MOD_ProDKin_1 | 112 | 118 | PF00069 | 0.622 |
MOD_ProDKin_1 | 138 | 144 | PF00069 | 0.723 |
MOD_ProDKin_1 | 156 | 162 | PF00069 | 0.556 |
MOD_ProDKin_1 | 181 | 187 | PF00069 | 0.484 |
MOD_ProDKin_1 | 227 | 233 | PF00069 | 0.690 |
MOD_ProDKin_1 | 251 | 257 | PF00069 | 0.714 |
MOD_ProDKin_1 | 277 | 283 | PF00069 | 0.584 |
MOD_ProDKin_1 | 314 | 320 | PF00069 | 0.553 |
MOD_ProDKin_1 | 351 | 357 | PF00069 | 0.583 |
MOD_ProDKin_1 | 408 | 414 | PF00069 | 0.329 |
MOD_ProDKin_1 | 477 | 483 | PF00069 | 0.476 |
MOD_ProDKin_1 | 550 | 556 | PF00069 | 0.419 |
MOD_ProDKin_1 | 615 | 621 | PF00069 | 0.591 |
TRG_DiLeu_BaEn_1 | 362 | 367 | PF01217 | 0.483 |
TRG_DiLeu_BaEn_2 | 561 | 567 | PF01217 | 0.364 |
TRG_DiLeu_BaLyEn_6 | 511 | 516 | PF01217 | 0.459 |
TRG_DiLeu_LyEn_5 | 362 | 367 | PF01217 | 0.433 |
TRG_ENDOCYTIC_2 | 208 | 211 | PF00928 | 0.481 |
TRG_ENDOCYTIC_2 | 330 | 333 | PF00928 | 0.661 |
TRG_ENDOCYTIC_2 | 379 | 382 | PF00928 | 0.429 |
TRG_ENDOCYTIC_2 | 455 | 458 | PF00928 | 0.414 |
TRG_ENDOCYTIC_2 | 561 | 564 | PF00928 | 0.361 |
TRG_ENDOCYTIC_2 | 573 | 576 | PF00928 | 0.444 |
TRG_ER_diArg_1 | 17 | 20 | PF00400 | 0.594 |
TRG_ER_diArg_1 | 2 | 5 | PF00400 | 0.615 |
TRG_ER_diArg_1 | 211 | 214 | PF00400 | 0.536 |
TRG_ER_diArg_1 | 363 | 365 | PF00400 | 0.447 |
TRG_ER_diArg_1 | 526 | 529 | PF00400 | 0.361 |
TRG_ER_diArg_1 | 99 | 102 | PF00400 | 0.681 |
TRG_Pf-PMV_PEXEL_1 | 471 | 475 | PF00026 | 0.607 |
TRG_Pf-PMV_PEXEL_1 | 558 | 562 | PF00026 | 0.459 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HYY8 | Leptomonas seymouri | 52% | 74% |
A0A3S7WYC3 | Leishmania donovani | 86% | 81% |
A4HDI0 | Leishmania braziliensis | 74% | 100% |
A4I0W1 | Leishmania infantum | 86% | 81% |
Q4QAK9 | Leishmania major | 86% | 100% |