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: 12 |
NetGPI | no | yes: 0, no: 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005840 | ribosome | 5 | 13 |
GO:0032991 | protein-containing complex | 1 | 13 |
GO:0043226 | organelle | 2 | 13 |
GO:0043228 | non-membrane-bounded organelle | 3 | 13 |
GO:0043229 | intracellular organelle | 3 | 13 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 13 |
GO:0110165 | cellular anatomical entity | 1 | 13 |
GO:1990904 | ribonucleoprotein complex | 2 | 13 |
GO:0005815 | microtubule organizing center | 2 | 1 |
GO:0036064 | ciliary basal body | 3 | 1 |
GO:0005730 | nucleolus | 5 | 5 |
Related structures:
AlphaFold database: A4HAG2
Term | Name | Level | Count |
---|---|---|---|
GO:0000027 | ribosomal large subunit assembly | 7 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0022607 | cellular component assembly | 4 | 1 |
GO:0022618 | ribonucleoprotein complex assembly | 6 | 1 |
GO:0043933 | protein-containing complex organization | 4 | 1 |
GO:0065003 | protein-containing complex assembly | 5 | 1 |
GO:0071826 | ribonucleoprotein complex subunit organization | 5 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 107 | 109 | PF00675 | 0.586 |
CLV_NRD_NRD_1 | 275 | 277 | PF00675 | 0.407 |
CLV_NRD_NRD_1 | 294 | 296 | PF00675 | 0.707 |
CLV_NRD_NRD_1 | 411 | 413 | PF00675 | 0.530 |
CLV_NRD_NRD_1 | 513 | 515 | PF00675 | 0.732 |
CLV_PCSK_KEX2_1 | 107 | 109 | PF00082 | 0.586 |
CLV_PCSK_KEX2_1 | 275 | 277 | PF00082 | 0.407 |
CLV_PCSK_KEX2_1 | 294 | 296 | PF00082 | 0.707 |
CLV_PCSK_SKI1_1 | 155 | 159 | PF00082 | 0.351 |
CLV_PCSK_SKI1_1 | 373 | 377 | PF00082 | 0.330 |
CLV_PCSK_SKI1_1 | 434 | 438 | PF00082 | 0.514 |
CLV_PCSK_SKI1_1 | 498 | 502 | PF00082 | 0.521 |
CLV_PCSK_SKI1_1 | 541 | 545 | PF00082 | 0.509 |
CLV_PCSK_SKI1_1 | 668 | 672 | PF00082 | 0.385 |
DEG_SCF_FBW7_1 | 280 | 286 | PF00400 | 0.481 |
DEG_SPOP_SBC_1 | 185 | 189 | PF00917 | 0.579 |
DEG_SPOP_SBC_1 | 208 | 212 | PF00917 | 0.498 |
DOC_CKS1_1 | 280 | 285 | PF01111 | 0.479 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 647 | 655 | PF00134 | 0.476 |
DOC_MAPK_gen_1 | 233 | 242 | PF00069 | 0.334 |
DOC_MAPK_MEF2A_6 | 233 | 242 | PF00069 | 0.317 |
DOC_MAPK_MEF2A_6 | 505 | 512 | PF00069 | 0.522 |
DOC_PP1_RVXF_1 | 134 | 141 | PF00149 | 0.396 |
DOC_PP1_RVXF_1 | 410 | 417 | PF00149 | 0.567 |
DOC_PP2B_LxvP_1 | 101 | 104 | PF13499 | 0.554 |
DOC_PP2B_LxvP_1 | 701 | 704 | PF13499 | 0.461 |
DOC_PP4_FxxP_1 | 11 | 14 | PF00568 | 0.447 |
DOC_PP4_FxxP_1 | 183 | 186 | PF00568 | 0.390 |
DOC_USP7_MATH_1 | 165 | 169 | PF00917 | 0.619 |
DOC_USP7_MATH_1 | 184 | 188 | PF00917 | 0.410 |
DOC_USP7_MATH_1 | 204 | 208 | PF00917 | 0.402 |
DOC_USP7_MATH_1 | 281 | 285 | PF00917 | 0.558 |
DOC_USP7_MATH_1 | 352 | 356 | PF00917 | 0.513 |
DOC_USP7_MATH_1 | 448 | 452 | PF00917 | 0.555 |
DOC_USP7_MATH_1 | 457 | 461 | PF00917 | 0.712 |
DOC_USP7_MATH_1 | 491 | 495 | PF00917 | 0.605 |
DOC_USP7_MATH_1 | 499 | 503 | PF00917 | 0.544 |
DOC_USP7_MATH_1 | 535 | 539 | PF00917 | 0.546 |
DOC_USP7_MATH_1 | 570 | 574 | PF00917 | 0.601 |
DOC_USP7_MATH_1 | 654 | 658 | PF00917 | 0.495 |
DOC_WW_Pin1_4 | 279 | 284 | PF00397 | 0.514 |
DOC_WW_Pin1_4 | 287 | 292 | PF00397 | 0.538 |
DOC_WW_Pin1_4 | 37 | 42 | PF00397 | 0.542 |
DOC_WW_Pin1_4 | 406 | 411 | PF00397 | 0.664 |
DOC_WW_Pin1_4 | 453 | 458 | PF00397 | 0.659 |
DOC_WW_Pin1_4 | 517 | 522 | PF00397 | 0.645 |
DOC_WW_Pin1_4 | 81 | 86 | PF00397 | 0.508 |
LIG_14-3-3_CanoR_1 | 107 | 115 | PF00244 | 0.604 |
LIG_14-3-3_CanoR_1 | 245 | 249 | PF00244 | 0.391 |
LIG_14-3-3_CanoR_1 | 275 | 281 | PF00244 | 0.522 |
LIG_14-3-3_CanoR_1 | 294 | 300 | PF00244 | 0.689 |
LIG_14-3-3_CanoR_1 | 357 | 365 | PF00244 | 0.427 |
LIG_14-3-3_CanoR_1 | 434 | 442 | PF00244 | 0.574 |
LIG_14-3-3_CanoR_1 | 679 | 687 | PF00244 | 0.497 |
LIG_Actin_WH2_2 | 655 | 670 | PF00022 | 0.360 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.576 |
LIG_BIR_III_4 | 264 | 268 | PF00653 | 0.498 |
LIG_BRCT_BRCA1_1 | 210 | 214 | PF00533 | 0.498 |
LIG_BRCT_BRCA1_1 | 249 | 253 | PF00533 | 0.461 |
LIG_BRCT_BRCA1_1 | 31 | 35 | PF00533 | 0.502 |
LIG_BRCT_BRCA1_1 | 354 | 358 | PF00533 | 0.502 |
LIG_CSL_BTD_1 | 101 | 104 | PF09270 | 0.513 |
LIG_eIF4E_1 | 560 | 566 | PF01652 | 0.496 |
LIG_EVH1_2 | 521 | 525 | PF00568 | 0.534 |
LIG_FHA_1 | 110 | 116 | PF00498 | 0.687 |
LIG_FHA_1 | 200 | 206 | PF00498 | 0.502 |
LIG_FHA_1 | 329 | 335 | PF00498 | 0.616 |
LIG_FHA_1 | 372 | 378 | PF00498 | 0.502 |
LIG_FHA_1 | 394 | 400 | PF00498 | 0.489 |
LIG_FHA_1 | 594 | 600 | PF00498 | 0.624 |
LIG_LIR_Apic_2 | 182 | 186 | PF02991 | 0.380 |
LIG_LIR_Gen_1 | 212 | 219 | PF02991 | 0.498 |
LIG_LIR_Gen_1 | 632 | 643 | PF02991 | 0.488 |
LIG_LIR_Gen_1 | 96 | 104 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 2 | 6 | PF02991 | 0.577 |
LIG_LIR_Nem_3 | 211 | 217 | PF02991 | 0.498 |
LIG_LIR_Nem_3 | 632 | 638 | PF02991 | 0.490 |
LIG_LIR_Nem_3 | 92 | 98 | PF02991 | 0.475 |
LIG_MLH1_MIPbox_1 | 211 | 215 | PF16413 | 0.498 |
LIG_MYND_1 | 37 | 41 | PF01753 | 0.498 |
LIG_Pex14_1 | 160 | 164 | PF04695 | 0.443 |
LIG_Pex14_2 | 179 | 183 | PF04695 | 0.401 |
LIG_Rb_pABgroove_1 | 236 | 244 | PF01858 | 0.420 |
LIG_SH2_CRK | 343 | 347 | PF00017 | 0.293 |
LIG_SH2_CRK | 635 | 639 | PF00017 | 0.485 |
LIG_SH2_PTP2 | 98 | 101 | PF00017 | 0.502 |
LIG_SH2_STAP1 | 687 | 691 | PF00017 | 0.471 |
LIG_SH2_STAT5 | 147 | 150 | PF00017 | 0.348 |
LIG_SH2_STAT5 | 209 | 212 | PF00017 | 0.501 |
LIG_SH2_STAT5 | 217 | 220 | PF00017 | 0.503 |
LIG_SH2_STAT5 | 258 | 261 | PF00017 | 0.493 |
LIG_SH2_STAT5 | 341 | 344 | PF00017 | 0.372 |
LIG_SH2_STAT5 | 564 | 567 | PF00017 | 0.627 |
LIG_SH2_STAT5 | 98 | 101 | PF00017 | 0.525 |
LIG_SH3_3 | 11 | 17 | PF00018 | 0.441 |
LIG_SH3_3 | 40 | 46 | PF00018 | 0.498 |
LIG_SH3_3 | 503 | 509 | PF00018 | 0.507 |
LIG_SH3_3 | 518 | 524 | PF00018 | 0.548 |
LIG_SUMO_SIM_par_1 | 201 | 207 | PF11976 | 0.502 |
LIG_TRAF2_1 | 619 | 622 | PF00917 | 0.510 |
LIG_WRC_WIRS_1 | 180 | 185 | PF05994 | 0.469 |
LIG_WW_2 | 506 | 509 | PF00397 | 0.526 |
MOD_CDK_SPK_2 | 453 | 458 | PF00069 | 0.598 |
MOD_CDK_SPK_2 | 81 | 86 | PF00069 | 0.498 |
MOD_CDK_SPxK_1 | 406 | 412 | PF00069 | 0.493 |
MOD_CDK_SPxxK_3 | 287 | 294 | PF00069 | 0.483 |
MOD_CDK_SPxxK_3 | 406 | 413 | PF00069 | 0.560 |
MOD_CK1_1 | 207 | 213 | PF00069 | 0.539 |
MOD_CK1_1 | 247 | 253 | PF00069 | 0.506 |
MOD_CK1_1 | 279 | 285 | PF00069 | 0.609 |
MOD_CK1_1 | 427 | 433 | PF00069 | 0.511 |
MOD_CK1_1 | 451 | 457 | PF00069 | 0.620 |
MOD_CK1_1 | 464 | 470 | PF00069 | 0.732 |
MOD_CK1_1 | 593 | 599 | PF00069 | 0.577 |
MOD_CK1_1 | 612 | 618 | PF00069 | 0.483 |
MOD_CK1_1 | 657 | 663 | PF00069 | 0.354 |
MOD_CK2_1 | 388 | 394 | PF00069 | 0.605 |
MOD_CK2_1 | 517 | 523 | PF00069 | 0.623 |
MOD_CK2_1 | 716 | 722 | PF00069 | 0.513 |
MOD_GlcNHglycan | 206 | 209 | PF01048 | 0.307 |
MOD_GlcNHglycan | 219 | 222 | PF01048 | 0.264 |
MOD_GlcNHglycan | 261 | 264 | PF01048 | 0.276 |
MOD_GlcNHglycan | 265 | 268 | PF01048 | 0.302 |
MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.645 |
MOD_GlcNHglycan | 324 | 327 | PF01048 | 0.305 |
MOD_GlcNHglycan | 379 | 382 | PF01048 | 0.372 |
MOD_GlcNHglycan | 416 | 419 | PF01048 | 0.662 |
MOD_GlcNHglycan | 450 | 453 | PF01048 | 0.596 |
MOD_GlcNHglycan | 459 | 462 | PF01048 | 0.724 |
MOD_GlcNHglycan | 463 | 466 | PF01048 | 0.765 |
MOD_GlcNHglycan | 476 | 479 | PF01048 | 0.669 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.263 |
MOD_GlcNHglycan | 537 | 540 | PF01048 | 0.529 |
MOD_GlcNHglycan | 572 | 575 | PF01048 | 0.574 |
MOD_GlcNHglycan | 592 | 595 | PF01048 | 0.808 |
MOD_GlcNHglycan | 611 | 614 | PF01048 | 0.552 |
MOD_GlcNHglycan | 709 | 712 | PF01048 | 0.587 |
MOD_GlcNHglycan | 91 | 94 | PF01048 | 0.302 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.509 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.532 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.538 |
MOD_GSK3_1 | 275 | 282 | PF00069 | 0.626 |
MOD_GSK3_1 | 283 | 290 | PF00069 | 0.574 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.468 |
MOD_GSK3_1 | 352 | 359 | PF00069 | 0.461 |
MOD_GSK3_1 | 388 | 395 | PF00069 | 0.606 |
MOD_GSK3_1 | 423 | 430 | PF00069 | 0.576 |
MOD_GSK3_1 | 453 | 460 | PF00069 | 0.636 |
MOD_GSK3_1 | 551 | 558 | PF00069 | 0.738 |
MOD_GSK3_1 | 589 | 596 | PF00069 | 0.612 |
MOD_GSK3_1 | 608 | 615 | PF00069 | 0.481 |
MOD_GSK3_1 | 657 | 664 | PF00069 | 0.446 |
MOD_GSK3_1 | 673 | 680 | PF00069 | 0.452 |
MOD_GSK3_1 | 707 | 714 | PF00069 | 0.541 |
MOD_N-GLC_1 | 327 | 332 | PF02516 | 0.298 |
MOD_N-GLC_1 | 434 | 439 | PF02516 | 0.517 |
MOD_N-GLC_1 | 491 | 496 | PF02516 | 0.630 |
MOD_N-GLC_1 | 578 | 583 | PF02516 | 0.540 |
MOD_N-GLC_1 | 609 | 614 | PF02516 | 0.456 |
MOD_N-GLC_1 | 711 | 716 | PF02516 | 0.482 |
MOD_N-GLC_2 | 124 | 126 | PF02516 | 0.501 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.579 |
MOD_NEK2_1 | 179 | 184 | PF00069 | 0.469 |
MOD_NEK2_1 | 342 | 347 | PF00069 | 0.359 |
MOD_NEK2_1 | 423 | 428 | PF00069 | 0.544 |
MOD_NEK2_1 | 543 | 548 | PF00069 | 0.505 |
MOD_NEK2_1 | 565 | 570 | PF00069 | 0.625 |
MOD_NEK2_1 | 716 | 721 | PF00069 | 0.510 |
MOD_NEK2_1 | 89 | 94 | PF00069 | 0.473 |
MOD_NEK2_2 | 244 | 249 | PF00069 | 0.328 |
MOD_NEK2_2 | 352 | 357 | PF00069 | 0.450 |
MOD_NEK2_2 | 595 | 600 | PF00069 | 0.603 |
MOD_PIKK_1 | 165 | 171 | PF00454 | 0.559 |
MOD_PIKK_1 | 427 | 433 | PF00454 | 0.604 |
MOD_PIKK_1 | 434 | 440 | PF00454 | 0.536 |
MOD_PIKK_1 | 459 | 465 | PF00454 | 0.677 |
MOD_PIKK_1 | 661 | 667 | PF00454 | 0.366 |
MOD_PIKK_1 | 679 | 685 | PF00454 | 0.370 |
MOD_PK_1 | 544 | 550 | PF00069 | 0.501 |
MOD_PKA_1 | 107 | 113 | PF00069 | 0.590 |
MOD_PKA_1 | 275 | 281 | PF00069 | 0.474 |
MOD_PKA_1 | 294 | 300 | PF00069 | 0.683 |
MOD_PKA_2 | 106 | 112 | PF00069 | 0.537 |
MOD_PKA_2 | 122 | 128 | PF00069 | 0.496 |
MOD_PKA_2 | 15 | 21 | PF00069 | 0.457 |
MOD_PKA_2 | 244 | 250 | PF00069 | 0.483 |
MOD_PKA_2 | 275 | 281 | PF00069 | 0.573 |
MOD_PKA_2 | 294 | 300 | PF00069 | 0.358 |
MOD_PKA_2 | 356 | 362 | PF00069 | 0.427 |
MOD_PKA_2 | 448 | 454 | PF00069 | 0.533 |
MOD_PKB_1 | 677 | 685 | PF00069 | 0.379 |
MOD_Plk_1 | 153 | 159 | PF00069 | 0.404 |
MOD_Plk_1 | 371 | 377 | PF00069 | 0.502 |
MOD_Plk_1 | 393 | 399 | PF00069 | 0.523 |
MOD_Plk_1 | 491 | 497 | PF00069 | 0.593 |
MOD_Plk_1 | 544 | 550 | PF00069 | 0.690 |
MOD_Plk_1 | 551 | 557 | PF00069 | 0.593 |
MOD_Plk_1 | 578 | 584 | PF00069 | 0.542 |
MOD_Plk_1 | 711 | 717 | PF00069 | 0.485 |
MOD_Plk_4 | 210 | 216 | PF00069 | 0.498 |
MOD_Plk_4 | 295 | 301 | PF00069 | 0.540 |
MOD_Plk_4 | 371 | 377 | PF00069 | 0.502 |
MOD_Plk_4 | 508 | 514 | PF00069 | 0.538 |
MOD_Plk_4 | 544 | 550 | PF00069 | 0.569 |
MOD_Plk_4 | 657 | 663 | PF00069 | 0.378 |
MOD_ProDKin_1 | 279 | 285 | PF00069 | 0.516 |
MOD_ProDKin_1 | 287 | 293 | PF00069 | 0.536 |
MOD_ProDKin_1 | 37 | 43 | PF00069 | 0.542 |
MOD_ProDKin_1 | 406 | 412 | PF00069 | 0.666 |
MOD_ProDKin_1 | 453 | 459 | PF00069 | 0.660 |
MOD_ProDKin_1 | 517 | 523 | PF00069 | 0.647 |
MOD_ProDKin_1 | 81 | 87 | PF00069 | 0.508 |
MOD_SUMO_rev_2 | 330 | 340 | PF00179 | 0.498 |
MOD_SUMO_rev_2 | 528 | 538 | PF00179 | 0.584 |
MOD_SUMO_rev_2 | 688 | 697 | PF00179 | 0.467 |
TRG_DiLeu_BaEn_1 | 624 | 629 | PF01217 | 0.506 |
TRG_DiLeu_BaLyEn_6 | 40 | 45 | PF01217 | 0.498 |
TRG_ENDOCYTIC_2 | 343 | 346 | PF00928 | 0.348 |
TRG_ENDOCYTIC_2 | 635 | 638 | PF00928 | 0.488 |
TRG_ENDOCYTIC_2 | 98 | 101 | PF00928 | 0.528 |
TRG_ER_diArg_1 | 274 | 276 | PF00400 | 0.355 |
TRG_ER_diArg_1 | 293 | 295 | PF00400 | 0.735 |
TRG_ER_diArg_1 | 678 | 681 | PF00400 | 0.388 |
TRG_NES_CRM1_1 | 693 | 707 | PF08389 | 0.383 |
TRG_Pf-PMV_PEXEL_1 | 541 | 545 | PF00026 | 0.509 |
TRG_Pf-PMV_PEXEL_1 | 642 | 646 | PF00026 | 0.370 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PBY0 | Leptomonas seymouri | 41% | 100% |
A0A3Q8IGC4 | Leishmania donovani | 24% | 100% |
A0A3Q8IKN8 | Leishmania donovani | 77% | 100% |
A0A3R7NL29 | Trypanosoma rangeli | 35% | 98% |
A4HDT7 | Leishmania braziliensis | 24% | 100% |
A4I135 | Leishmania infantum | 24% | 100% |
A4I9L7 | Leishmania infantum | 76% | 100% |
E9AX72 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
E9B4L5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 76% | 100% |
Q4Q3G1 | Leishmania major | 76% | 100% |
Q4QAA4 | Leishmania major | 24% | 100% |