Uncharacterized Protein, Uncharacterized
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: A4ICF2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 302 | 306 | PF00656 | 0.590 |
CLV_C14_Caspase3-7 | 323 | 327 | PF00656 | 0.679 |
CLV_NRD_NRD_1 | 106 | 108 | PF00675 | 0.438 |
CLV_NRD_NRD_1 | 349 | 351 | PF00675 | 0.720 |
CLV_NRD_NRD_1 | 360 | 362 | PF00675 | 0.557 |
CLV_NRD_NRD_1 | 385 | 387 | PF00675 | 0.606 |
CLV_NRD_NRD_1 | 420 | 422 | PF00675 | 0.697 |
CLV_NRD_NRD_1 | 488 | 490 | PF00675 | 0.522 |
CLV_PCSK_KEX2_1 | 106 | 108 | PF00082 | 0.438 |
CLV_PCSK_KEX2_1 | 385 | 387 | PF00082 | 0.606 |
CLV_PCSK_KEX2_1 | 392 | 394 | PF00082 | 0.480 |
CLV_PCSK_KEX2_1 | 420 | 422 | PF00082 | 0.694 |
CLV_PCSK_KEX2_1 | 488 | 490 | PF00082 | 0.522 |
CLV_PCSK_PC1ET2_1 | 392 | 394 | PF00082 | 0.336 |
CLV_PCSK_PC7_1 | 381 | 387 | PF00082 | 0.573 |
CLV_PCSK_SKI1_1 | 119 | 123 | PF00082 | 0.362 |
CLV_PCSK_SKI1_1 | 371 | 375 | PF00082 | 0.524 |
CLV_PCSK_SKI1_1 | 386 | 390 | PF00082 | 0.418 |
CLV_PCSK_SKI1_1 | 451 | 455 | PF00082 | 0.511 |
CLV_PCSK_SKI1_1 | 526 | 530 | PF00082 | 0.539 |
CLV_PCSK_SKI1_1 | 558 | 562 | PF00082 | 0.583 |
CLV_PCSK_SKI1_1 | 582 | 586 | PF00082 | 0.409 |
CLV_Separin_Metazoa | 523 | 527 | PF03568 | 0.435 |
DEG_APCC_DBOX_1 | 525 | 533 | PF00400 | 0.469 |
DEG_APCC_DBOX_1 | 581 | 589 | PF00400 | 0.409 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.442 |
DOC_ANK_TNKS_1 | 270 | 277 | PF00023 | 0.569 |
DOC_CYCLIN_yCln2_LP_2 | 498 | 504 | PF00134 | 0.502 |
DOC_MAPK_gen_1 | 134 | 143 | PF00069 | 0.459 |
DOC_MAPK_gen_1 | 392 | 399 | PF00069 | 0.381 |
DOC_MAPK_gen_1 | 655 | 665 | PF00069 | 0.483 |
DOC_MAPK_MEF2A_6 | 137 | 145 | PF00069 | 0.426 |
DOC_MAPK_MEF2A_6 | 477 | 486 | PF00069 | 0.446 |
DOC_MAPK_MEF2A_6 | 582 | 590 | PF00069 | 0.520 |
DOC_PP1_RVXF_1 | 364 | 371 | PF00149 | 0.503 |
DOC_PP1_RVXF_1 | 384 | 391 | PF00149 | 0.539 |
DOC_PP2B_LxvP_1 | 79 | 82 | PF13499 | 0.580 |
DOC_PP4_FxxP_1 | 445 | 448 | PF00568 | 0.526 |
DOC_USP7_MATH_1 | 205 | 209 | PF00917 | 0.568 |
DOC_USP7_MATH_1 | 315 | 319 | PF00917 | 0.670 |
DOC_USP7_MATH_1 | 331 | 335 | PF00917 | 0.542 |
DOC_USP7_MATH_1 | 502 | 506 | PF00917 | 0.379 |
DOC_USP7_MATH_1 | 55 | 59 | PF00917 | 0.526 |
DOC_USP7_MATH_1 | 74 | 78 | PF00917 | 0.486 |
DOC_USP7_UBL2_3 | 362 | 366 | PF12436 | 0.526 |
DOC_WW_Pin1_4 | 223 | 228 | PF00397 | 0.578 |
DOC_WW_Pin1_4 | 259 | 264 | PF00397 | 0.378 |
DOC_WW_Pin1_4 | 265 | 270 | PF00397 | 0.501 |
DOC_WW_Pin1_4 | 404 | 409 | PF00397 | 0.576 |
DOC_WW_Pin1_4 | 454 | 459 | PF00397 | 0.685 |
DOC_WW_Pin1_4 | 558 | 563 | PF00397 | 0.757 |
DOC_WW_Pin1_4 | 88 | 93 | PF00397 | 0.677 |
LIG_14-3-3_CanoR_1 | 111 | 117 | PF00244 | 0.470 |
LIG_14-3-3_CanoR_1 | 22 | 26 | PF00244 | 0.569 |
LIG_14-3-3_CanoR_1 | 220 | 226 | PF00244 | 0.580 |
LIG_14-3-3_CanoR_1 | 385 | 391 | PF00244 | 0.444 |
LIG_14-3-3_CanoR_1 | 451 | 459 | PF00244 | 0.498 |
LIG_14-3-3_CanoR_1 | 517 | 521 | PF00244 | 0.523 |
LIG_14-3-3_CanoR_1 | 618 | 622 | PF00244 | 0.437 |
LIG_14-3-3_CanoR_1 | 633 | 639 | PF00244 | 0.523 |
LIG_BIR_III_2 | 305 | 309 | PF00653 | 0.674 |
LIG_CtBP_PxDLS_1 | 458 | 462 | PF00389 | 0.551 |
LIG_FHA_1 | 341 | 347 | PF00498 | 0.585 |
LIG_FHA_1 | 454 | 460 | PF00498 | 0.520 |
LIG_FHA_1 | 506 | 512 | PF00498 | 0.441 |
LIG_FHA_1 | 58 | 64 | PF00498 | 0.536 |
LIG_FHA_1 | 593 | 599 | PF00498 | 0.409 |
LIG_FHA_1 | 640 | 646 | PF00498 | 0.423 |
LIG_FHA_1 | 675 | 681 | PF00498 | 0.640 |
LIG_FHA_2 | 321 | 327 | PF00498 | 0.677 |
LIG_LIR_Apic_2 | 644 | 650 | PF02991 | 0.532 |
LIG_LIR_Gen_1 | 463 | 468 | PF02991 | 0.601 |
LIG_LIR_Nem_3 | 235 | 240 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 24 | 28 | PF02991 | 0.578 |
LIG_LIR_Nem_3 | 463 | 467 | PF02991 | 0.621 |
LIG_LIR_Nem_3 | 620 | 624 | PF02991 | 0.573 |
LIG_LYPXL_yS_3 | 670 | 673 | PF13949 | 0.492 |
LIG_NRBOX | 584 | 590 | PF00104 | 0.515 |
LIG_PCNA_yPIPBox_3 | 172 | 184 | PF02747 | 0.418 |
LIG_SH2_NCK_1 | 298 | 302 | PF00017 | 0.564 |
LIG_SH2_NCK_1 | 536 | 540 | PF00017 | 0.438 |
LIG_SH2_SRC | 298 | 301 | PF00017 | 0.564 |
LIG_SH2_SRC | 536 | 539 | PF00017 | 0.554 |
LIG_SH2_STAP1 | 254 | 258 | PF00017 | 0.475 |
LIG_SH2_STAP1 | 479 | 483 | PF00017 | 0.525 |
LIG_SH2_STAT5 | 131 | 134 | PF00017 | 0.465 |
LIG_SH2_STAT5 | 170 | 173 | PF00017 | 0.467 |
LIG_SH2_STAT5 | 237 | 240 | PF00017 | 0.398 |
LIG_SH2_STAT5 | 68 | 71 | PF00017 | 0.365 |
LIG_SH3_3 | 333 | 339 | PF00018 | 0.598 |
LIG_SH3_3 | 440 | 446 | PF00018 | 0.513 |
LIG_SH3_3 | 89 | 95 | PF00018 | 0.584 |
LIG_Sin3_3 | 480 | 487 | PF02671 | 0.347 |
LIG_SUMO_SIM_anti_2 | 512 | 517 | PF11976 | 0.524 |
LIG_SUMO_SIM_par_1 | 454 | 463 | PF11976 | 0.619 |
LIG_SUMO_SIM_par_1 | 58 | 66 | PF11976 | 0.523 |
LIG_TRAF2_1 | 623 | 626 | PF00917 | 0.553 |
LIG_TRFH_1 | 259 | 263 | PF08558 | 0.441 |
LIG_UBA3_1 | 28 | 32 | PF00899 | 0.583 |
LIG_WRC_WIRS_1 | 461 | 466 | PF05994 | 0.612 |
MOD_CDC14_SPxK_1 | 268 | 271 | PF00782 | 0.565 |
MOD_CDC14_SPxK_1 | 91 | 94 | PF00782 | 0.691 |
MOD_CDK_SPK_2 | 404 | 409 | PF00069 | 0.576 |
MOD_CDK_SPxK_1 | 265 | 271 | PF00069 | 0.529 |
MOD_CDK_SPxK_1 | 88 | 94 | PF00069 | 0.682 |
MOD_CK1_1 | 162 | 168 | PF00069 | 0.555 |
MOD_CK1_1 | 208 | 214 | PF00069 | 0.572 |
MOD_CK1_1 | 24 | 30 | PF00069 | 0.423 |
MOD_CK1_1 | 265 | 271 | PF00069 | 0.624 |
MOD_CK1_1 | 430 | 436 | PF00069 | 0.695 |
MOD_CK1_1 | 460 | 466 | PF00069 | 0.614 |
MOD_CK1_1 | 505 | 511 | PF00069 | 0.424 |
MOD_CK1_1 | 632 | 638 | PF00069 | 0.510 |
MOD_CK1_1 | 641 | 647 | PF00069 | 0.479 |
MOD_CK1_1 | 8 | 14 | PF00069 | 0.559 |
MOD_CK2_1 | 102 | 108 | PF00069 | 0.518 |
MOD_CK2_1 | 112 | 118 | PF00069 | 0.345 |
MOD_CK2_1 | 374 | 380 | PF00069 | 0.525 |
MOD_Cter_Amidation | 418 | 421 | PF01082 | 0.633 |
MOD_GlcNHglycan | 161 | 164 | PF01048 | 0.525 |
MOD_GlcNHglycan | 207 | 210 | PF01048 | 0.438 |
MOD_GlcNHglycan | 255 | 258 | PF01048 | 0.404 |
MOD_GlcNHglycan | 309 | 312 | PF01048 | 0.692 |
MOD_GlcNHglycan | 326 | 329 | PF01048 | 0.562 |
MOD_GlcNHglycan | 416 | 419 | PF01048 | 0.531 |
MOD_GlcNHglycan | 436 | 439 | PF01048 | 0.534 |
MOD_GlcNHglycan | 474 | 477 | PF01048 | 0.559 |
MOD_GlcNHglycan | 651 | 654 | PF01048 | 0.411 |
MOD_GlcNHglycan | 76 | 79 | PF01048 | 0.464 |
MOD_GSK3_1 | 179 | 186 | PF00069 | 0.405 |
MOD_GSK3_1 | 223 | 230 | PF00069 | 0.590 |
MOD_GSK3_1 | 320 | 327 | PF00069 | 0.651 |
MOD_GSK3_1 | 426 | 433 | PF00069 | 0.638 |
MOD_GSK3_1 | 453 | 460 | PF00069 | 0.622 |
MOD_GSK3_1 | 466 | 473 | PF00069 | 0.487 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.538 |
MOD_GSK3_1 | 505 | 512 | PF00069 | 0.590 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.464 |
MOD_GSK3_1 | 634 | 641 | PF00069 | 0.490 |
MOD_GSK3_1 | 645 | 652 | PF00069 | 0.367 |
MOD_N-GLC_1 | 502 | 507 | PF02516 | 0.371 |
MOD_NEK2_1 | 136 | 141 | PF00069 | 0.426 |
MOD_NEK2_1 | 21 | 26 | PF00069 | 0.588 |
MOD_NEK2_1 | 412 | 417 | PF00069 | 0.567 |
MOD_NEK2_1 | 453 | 458 | PF00069 | 0.511 |
MOD_NEK2_1 | 545 | 550 | PF00069 | 0.480 |
MOD_NEK2_1 | 598 | 603 | PF00069 | 0.492 |
MOD_NEK2_1 | 638 | 643 | PF00069 | 0.559 |
MOD_NEK2_1 | 675 | 680 | PF00069 | 0.578 |
MOD_NEK2_2 | 502 | 507 | PF00069 | 0.371 |
MOD_PIKK_1 | 208 | 214 | PF00454 | 0.541 |
MOD_PIKK_1 | 262 | 268 | PF00454 | 0.501 |
MOD_PIKK_1 | 545 | 551 | PF00454 | 0.492 |
MOD_PKA_2 | 136 | 142 | PF00069 | 0.544 |
MOD_PKA_2 | 205 | 211 | PF00069 | 0.445 |
MOD_PKA_2 | 21 | 27 | PF00069 | 0.561 |
MOD_PKA_2 | 516 | 522 | PF00069 | 0.524 |
MOD_PKA_2 | 617 | 623 | PF00069 | 0.440 |
MOD_PKA_2 | 632 | 638 | PF00069 | 0.522 |
MOD_PKA_2 | 83 | 89 | PF00069 | 0.601 |
MOD_PKA_2 | 93 | 99 | PF00069 | 0.640 |
MOD_Plk_1 | 426 | 432 | PF00069 | 0.650 |
MOD_Plk_1 | 502 | 508 | PF00069 | 0.488 |
MOD_Plk_1 | 509 | 515 | PF00069 | 0.499 |
MOD_Plk_1 | 675 | 681 | PF00069 | 0.500 |
MOD_Plk_2-3 | 575 | 581 | PF00069 | 0.545 |
MOD_Plk_4 | 24 | 30 | PF00069 | 0.627 |
MOD_Plk_4 | 331 | 337 | PF00069 | 0.541 |
MOD_Plk_4 | 374 | 380 | PF00069 | 0.634 |
MOD_Plk_4 | 42 | 48 | PF00069 | 0.289 |
MOD_Plk_4 | 427 | 433 | PF00069 | 0.714 |
MOD_Plk_4 | 502 | 508 | PF00069 | 0.427 |
MOD_Plk_4 | 516 | 522 | PF00069 | 0.457 |
MOD_Plk_4 | 617 | 623 | PF00069 | 0.504 |
MOD_Plk_4 | 63 | 69 | PF00069 | 0.477 |
MOD_Plk_4 | 675 | 681 | PF00069 | 0.522 |
MOD_ProDKin_1 | 223 | 229 | PF00069 | 0.576 |
MOD_ProDKin_1 | 259 | 265 | PF00069 | 0.384 |
MOD_ProDKin_1 | 404 | 410 | PF00069 | 0.579 |
MOD_ProDKin_1 | 454 | 460 | PF00069 | 0.685 |
MOD_ProDKin_1 | 558 | 564 | PF00069 | 0.760 |
MOD_ProDKin_1 | 88 | 94 | PF00069 | 0.682 |
MOD_SUMO_for_1 | 31 | 34 | PF00179 | 0.488 |
MOD_SUMO_rev_2 | 355 | 363 | PF00179 | 0.534 |
TRG_DiLeu_BaEn_1 | 243 | 248 | PF01217 | 0.496 |
TRG_DiLeu_BaLyEn_6 | 116 | 121 | PF01217 | 0.434 |
TRG_DiLeu_BaLyEn_6 | 141 | 146 | PF01217 | 0.409 |
TRG_DiLeu_BaLyEn_6 | 448 | 453 | PF01217 | 0.589 |
TRG_ENDOCYTIC_2 | 479 | 482 | PF00928 | 0.426 |
TRG_ENDOCYTIC_2 | 536 | 539 | PF00928 | 0.524 |
TRG_ENDOCYTIC_2 | 670 | 673 | PF00928 | 0.623 |
TRG_ER_diArg_1 | 420 | 422 | PF00400 | 0.691 |
TRG_Pf-PMV_PEXEL_1 | 134 | 138 | PF00026 | 0.451 |
TRG_Pf-PMV_PEXEL_1 | 420 | 424 | PF00026 | 0.546 |
TRG_Pf-PMV_PEXEL_1 | 451 | 455 | PF00026 | 0.591 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PBJ6 | Leptomonas seymouri | 37% | 100% |
A0A3Q8INV1 | Leishmania donovani | 100% | 100% |
A4HPB2 | Leishmania braziliensis | 75% | 100% |
E9AT23 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
Q4Q1H5 | Leishmania major | 91% | 100% |