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: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9B6E1
Term | Name | Level | Count |
---|---|---|---|
GO:0006355 | regulation of DNA-templated transcription | 6 | 1 |
GO:0006357 | regulation of transcription by RNA polymerase II | 7 | 1 |
GO:0009889 | regulation of biosynthetic process | 4 | 1 |
GO:0010468 | regulation of gene expression | 5 | 1 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 1 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0031323 | regulation of cellular metabolic process | 4 | 1 |
GO:0031326 | regulation of cellular biosynthetic process | 5 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 1 |
GO:0051252 | regulation of RNA metabolic process | 5 | 1 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0080090 | regulation of primary metabolic process | 4 | 1 |
GO:1903506 | regulation of nucleic acid-templated transcription | 7 | 1 |
GO:2001141 | regulation of RNA biosynthetic process | 6 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 292 | 296 | PF00656 | 0.497 |
CLV_C14_Caspase3-7 | 738 | 742 | PF00656 | 0.700 |
CLV_NRD_NRD_1 | 165 | 167 | PF00675 | 0.453 |
CLV_NRD_NRD_1 | 236 | 238 | PF00675 | 0.798 |
CLV_NRD_NRD_1 | 324 | 326 | PF00675 | 0.491 |
CLV_NRD_NRD_1 | 336 | 338 | PF00675 | 0.419 |
CLV_NRD_NRD_1 | 446 | 448 | PF00675 | 0.683 |
CLV_NRD_NRD_1 | 525 | 527 | PF00675 | 0.544 |
CLV_NRD_NRD_1 | 531 | 533 | PF00675 | 0.522 |
CLV_NRD_NRD_1 | 586 | 588 | PF00675 | 0.605 |
CLV_NRD_NRD_1 | 88 | 90 | PF00675 | 0.544 |
CLV_PCSK_FUR_1 | 529 | 533 | PF00082 | 0.499 |
CLV_PCSK_KEX2_1 | 324 | 326 | PF00082 | 0.518 |
CLV_PCSK_KEX2_1 | 336 | 338 | PF00082 | 0.518 |
CLV_PCSK_KEX2_1 | 446 | 448 | PF00082 | 0.681 |
CLV_PCSK_KEX2_1 | 531 | 533 | PF00082 | 0.541 |
CLV_PCSK_KEX2_1 | 579 | 581 | PF00082 | 0.526 |
CLV_PCSK_KEX2_1 | 585 | 587 | PF00082 | 0.603 |
CLV_PCSK_KEX2_1 | 88 | 90 | PF00082 | 0.544 |
CLV_PCSK_KEX2_1 | 98 | 100 | PF00082 | 0.720 |
CLV_PCSK_PC1ET2_1 | 579 | 581 | PF00082 | 0.545 |
CLV_PCSK_PC1ET2_1 | 98 | 100 | PF00082 | 0.792 |
CLV_PCSK_PC7_1 | 84 | 90 | PF00082 | 0.521 |
CLV_PCSK_PC7_1 | 94 | 100 | PF00082 | 0.697 |
CLV_PCSK_SKI1_1 | 11 | 15 | PF00082 | 0.528 |
CLV_PCSK_SKI1_1 | 257 | 261 | PF00082 | 0.563 |
CLV_PCSK_SKI1_1 | 325 | 329 | PF00082 | 0.496 |
CLV_PCSK_SKI1_1 | 89 | 93 | PF00082 | 0.566 |
CLV_Separin_Metazoa | 363 | 367 | PF03568 | 0.514 |
DEG_APCC_DBOX_1 | 198 | 206 | PF00400 | 0.661 |
DEG_SPOP_SBC_1 | 435 | 439 | PF00917 | 0.692 |
DOC_CKS1_1 | 279 | 284 | PF01111 | 0.516 |
DOC_CKS1_1 | 368 | 373 | PF01111 | 0.580 |
DOC_CYCLIN_yCln2_LP_2 | 188 | 194 | PF00134 | 0.543 |
DOC_MAPK_gen_1 | 22 | 30 | PF00069 | 0.359 |
DOC_MAPK_gen_1 | 280 | 288 | PF00069 | 0.505 |
DOC_MAPK_gen_1 | 321 | 330 | PF00069 | 0.514 |
DOC_MAPK_gen_1 | 336 | 343 | PF00069 | 0.482 |
DOC_MAPK_gen_1 | 355 | 364 | PF00069 | 0.299 |
DOC_MAPK_gen_1 | 479 | 486 | PF00069 | 0.642 |
DOC_MAPK_gen_1 | 526 | 536 | PF00069 | 0.688 |
DOC_MAPK_MEF2A_6 | 271 | 279 | PF00069 | 0.404 |
DOC_MAPK_MEF2A_6 | 280 | 288 | PF00069 | 0.515 |
DOC_MAPK_MEF2A_6 | 3 | 12 | PF00069 | 0.430 |
DOC_PP1_RVXF_1 | 46 | 52 | PF00149 | 0.429 |
DOC_PP1_RVXF_1 | 7 | 13 | PF00149 | 0.476 |
DOC_PP4_FxxP_1 | 118 | 121 | PF00568 | 0.662 |
DOC_PP4_FxxP_1 | 279 | 282 | PF00568 | 0.526 |
DOC_PP4_FxxP_1 | 30 | 33 | PF00568 | 0.510 |
DOC_USP7_MATH_1 | 133 | 137 | PF00917 | 0.515 |
DOC_USP7_MATH_1 | 2 | 6 | PF00917 | 0.278 |
DOC_USP7_MATH_1 | 434 | 438 | PF00917 | 0.617 |
DOC_USP7_MATH_1 | 459 | 463 | PF00917 | 0.698 |
DOC_USP7_MATH_1 | 464 | 468 | PF00917 | 0.644 |
DOC_USP7_MATH_1 | 491 | 495 | PF00917 | 0.585 |
DOC_USP7_MATH_1 | 705 | 709 | PF00917 | 0.759 |
DOC_USP7_MATH_1 | 723 | 727 | PF00917 | 0.585 |
DOC_WW_Pin1_4 | 111 | 116 | PF00397 | 0.759 |
DOC_WW_Pin1_4 | 187 | 192 | PF00397 | 0.772 |
DOC_WW_Pin1_4 | 223 | 228 | PF00397 | 0.698 |
DOC_WW_Pin1_4 | 278 | 283 | PF00397 | 0.500 |
DOC_WW_Pin1_4 | 367 | 372 | PF00397 | 0.528 |
DOC_WW_Pin1_4 | 492 | 497 | PF00397 | 0.580 |
LIG_14-3-3_CanoR_1 | 3 | 7 | PF00244 | 0.275 |
LIG_14-3-3_CanoR_1 | 446 | 451 | PF00244 | 0.650 |
LIG_14-3-3_CanoR_1 | 55 | 62 | PF00244 | 0.308 |
LIG_14-3-3_CanoR_1 | 596 | 604 | PF00244 | 0.562 |
LIG_14-3-3_CanoR_1 | 660 | 668 | PF00244 | 0.504 |
LIG_14-3-3_CanoR_1 | 693 | 700 | PF00244 | 0.643 |
LIG_AP2alpha_2 | 683 | 685 | PF02296 | 0.621 |
LIG_Clathr_ClatBox_1 | 353 | 357 | PF01394 | 0.502 |
LIG_FHA_1 | 298 | 304 | PF00498 | 0.507 |
LIG_FHA_1 | 447 | 453 | PF00498 | 0.557 |
LIG_FHA_1 | 461 | 467 | PF00498 | 0.745 |
LIG_FHA_1 | 536 | 542 | PF00498 | 0.464 |
LIG_FHA_1 | 593 | 599 | PF00498 | 0.542 |
LIG_FHA_1 | 606 | 612 | PF00498 | 0.435 |
LIG_FHA_1 | 693 | 699 | PF00498 | 0.611 |
LIG_FHA_2 | 285 | 291 | PF00498 | 0.458 |
LIG_FHA_2 | 305 | 311 | PF00498 | 0.493 |
LIG_FHA_2 | 380 | 386 | PF00498 | 0.657 |
LIG_FHA_2 | 493 | 499 | PF00498 | 0.662 |
LIG_FHA_2 | 503 | 509 | PF00498 | 0.628 |
LIG_FHA_2 | 99 | 105 | PF00498 | 0.715 |
LIG_GBD_Chelix_1 | 635 | 643 | PF00786 | 0.440 |
LIG_Integrin_RGD_1 | 321 | 323 | PF01839 | 0.552 |
LIG_LIR_Apic_2 | 116 | 121 | PF02991 | 0.653 |
LIG_LIR_Apic_2 | 29 | 33 | PF02991 | 0.514 |
LIG_LIR_Apic_2 | 590 | 594 | PF02991 | 0.406 |
LIG_LIR_Apic_2 | 683 | 689 | PF02991 | 0.622 |
LIG_LIR_Gen_1 | 307 | 316 | PF02991 | 0.506 |
LIG_LIR_Gen_1 | 35 | 45 | PF02991 | 0.459 |
LIG_LIR_Gen_1 | 50 | 59 | PF02991 | 0.485 |
LIG_LIR_Gen_1 | 574 | 582 | PF02991 | 0.480 |
LIG_LIR_Gen_1 | 662 | 672 | PF02991 | 0.447 |
LIG_LIR_Gen_1 | 673 | 684 | PF02991 | 0.530 |
LIG_LIR_Gen_1 | 76 | 87 | PF02991 | 0.557 |
LIG_LIR_Nem_3 | 21 | 27 | PF02991 | 0.547 |
LIG_LIR_Nem_3 | 307 | 311 | PF02991 | 0.511 |
LIG_LIR_Nem_3 | 35 | 41 | PF02991 | 0.359 |
LIG_LIR_Nem_3 | 429 | 435 | PF02991 | 0.751 |
LIG_LIR_Nem_3 | 50 | 54 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 57 | 62 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 574 | 578 | PF02991 | 0.481 |
LIG_LIR_Nem_3 | 662 | 668 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 673 | 679 | PF02991 | 0.508 |
LIG_LIR_Nem_3 | 76 | 82 | PF02991 | 0.406 |
LIG_LYPXL_yS_3 | 432 | 435 | PF13949 | 0.691 |
LIG_PTAP_UEV_1 | 99 | 104 | PF05743 | 0.501 |
LIG_Rb_LxCxE_1 | 154 | 173 | PF01857 | 0.568 |
LIG_SH2_GRB2like | 676 | 679 | PF00017 | 0.513 |
LIG_SH2_STAT5 | 269 | 272 | PF00017 | 0.462 |
LIG_SH2_STAT5 | 334 | 337 | PF00017 | 0.451 |
LIG_SH2_STAT5 | 676 | 679 | PF00017 | 0.513 |
LIG_SH2_STAT5 | 78 | 81 | PF00017 | 0.467 |
LIG_SH3_1 | 94 | 100 | PF00018 | 0.691 |
LIG_SH3_3 | 10 | 16 | PF00018 | 0.487 |
LIG_SH3_3 | 240 | 246 | PF00018 | 0.565 |
LIG_SH3_3 | 493 | 499 | PF00018 | 0.613 |
LIG_SH3_3 | 610 | 616 | PF00018 | 0.491 |
LIG_SH3_3 | 681 | 687 | PF00018 | 0.585 |
LIG_SH3_3 | 94 | 100 | PF00018 | 0.691 |
LIG_SUMO_SIM_anti_2 | 695 | 701 | PF11976 | 0.661 |
LIG_SUMO_SIM_par_1 | 167 | 173 | PF11976 | 0.726 |
LIG_SUMO_SIM_par_1 | 379 | 385 | PF11976 | 0.711 |
LIG_SUMO_SIM_par_1 | 391 | 396 | PF11976 | 0.708 |
LIG_SUMO_SIM_par_1 | 695 | 701 | PF11976 | 0.563 |
LIG_UBA3_1 | 352 | 361 | PF00899 | 0.516 |
LIG_WRC_WIRS_1 | 27 | 32 | PF05994 | 0.582 |
LIG_WRC_WIRS_1 | 572 | 577 | PF05994 | 0.341 |
MOD_CDC14_SPxK_1 | 226 | 229 | PF00782 | 0.710 |
MOD_CDK_SPK_2 | 278 | 283 | PF00069 | 0.500 |
MOD_CDK_SPxK_1 | 223 | 229 | PF00069 | 0.711 |
MOD_CK1_1 | 138 | 144 | PF00069 | 0.740 |
MOD_CK1_1 | 182 | 188 | PF00069 | 0.567 |
MOD_CK1_1 | 437 | 443 | PF00069 | 0.684 |
MOD_CK1_1 | 548 | 554 | PF00069 | 0.501 |
MOD_CK1_1 | 57 | 63 | PF00069 | 0.503 |
MOD_CK2_1 | 26 | 32 | PF00069 | 0.581 |
MOD_CK2_1 | 284 | 290 | PF00069 | 0.472 |
MOD_CK2_1 | 304 | 310 | PF00069 | 0.482 |
MOD_CK2_1 | 357 | 363 | PF00069 | 0.483 |
MOD_CK2_1 | 379 | 385 | PF00069 | 0.657 |
MOD_CK2_1 | 47 | 53 | PF00069 | 0.436 |
MOD_CK2_1 | 492 | 498 | PF00069 | 0.642 |
MOD_CK2_1 | 713 | 719 | PF00069 | 0.645 |
MOD_CK2_1 | 98 | 104 | PF00069 | 0.709 |
MOD_GlcNHglycan | 128 | 131 | PF01048 | 0.805 |
MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.638 |
MOD_GlcNHglycan | 215 | 218 | PF01048 | 0.715 |
MOD_GlcNHglycan | 376 | 379 | PF01048 | 0.665 |
MOD_GlcNHglycan | 388 | 391 | PF01048 | 0.716 |
MOD_GlcNHglycan | 408 | 411 | PF01048 | 0.787 |
MOD_GlcNHglycan | 412 | 415 | PF01048 | 0.740 |
MOD_GlcNHglycan | 424 | 427 | PF01048 | 0.571 |
MOD_GlcNHglycan | 428 | 431 | PF01048 | 0.467 |
MOD_GlcNHglycan | 442 | 445 | PF01048 | 0.663 |
MOD_GlcNHglycan | 455 | 458 | PF01048 | 0.536 |
MOD_GlcNHglycan | 466 | 469 | PF01048 | 0.604 |
MOD_GlcNHglycan | 549 | 553 | PF01048 | 0.571 |
MOD_GlcNHglycan | 605 | 608 | PF01048 | 0.548 |
MOD_GlcNHglycan | 622 | 625 | PF01048 | 0.525 |
MOD_GlcNHglycan | 672 | 675 | PF01048 | 0.553 |
MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.528 |
MOD_GSK3_1 | 131 | 138 | PF00069 | 0.744 |
MOD_GSK3_1 | 219 | 226 | PF00069 | 0.691 |
MOD_GSK3_1 | 297 | 304 | PF00069 | 0.476 |
MOD_GSK3_1 | 406 | 413 | PF00069 | 0.784 |
MOD_GSK3_1 | 422 | 429 | PF00069 | 0.563 |
MOD_GSK3_1 | 434 | 441 | PF00069 | 0.562 |
MOD_GSK3_1 | 448 | 455 | PF00069 | 0.679 |
MOD_GSK3_1 | 460 | 467 | PF00069 | 0.609 |
MOD_GSK3_1 | 599 | 606 | PF00069 | 0.493 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.572 |
MOD_N-GLC_2 | 642 | 644 | PF02516 | 0.516 |
MOD_NEK2_1 | 180 | 185 | PF00069 | 0.587 |
MOD_NEK2_1 | 213 | 218 | PF00069 | 0.754 |
MOD_NEK2_1 | 356 | 361 | PF00069 | 0.526 |
MOD_NEK2_1 | 561 | 566 | PF00069 | 0.565 |
MOD_NEK2_1 | 597 | 602 | PF00069 | 0.512 |
MOD_NEK2_1 | 603 | 608 | PF00069 | 0.469 |
MOD_NEK2_2 | 379 | 384 | PF00069 | 0.711 |
MOD_NEK2_2 | 607 | 612 | PF00069 | 0.541 |
MOD_PIKK_1 | 297 | 303 | PF00454 | 0.521 |
MOD_PIKK_1 | 393 | 399 | PF00454 | 0.636 |
MOD_PIKK_1 | 535 | 541 | PF00454 | 0.531 |
MOD_PIKK_1 | 692 | 698 | PF00454 | 0.563 |
MOD_PKA_1 | 446 | 452 | PF00069 | 0.738 |
MOD_PKA_1 | 98 | 104 | PF00069 | 0.754 |
MOD_PKA_2 | 2 | 8 | PF00069 | 0.284 |
MOD_PKA_2 | 357 | 363 | PF00069 | 0.536 |
MOD_PKA_2 | 445 | 451 | PF00069 | 0.677 |
MOD_PKA_2 | 54 | 60 | PF00069 | 0.316 |
MOD_PKA_2 | 562 | 568 | PF00069 | 0.650 |
MOD_PKA_2 | 659 | 665 | PF00069 | 0.529 |
MOD_PKA_2 | 692 | 698 | PF00069 | 0.616 |
MOD_PKA_2 | 98 | 104 | PF00069 | 0.754 |
MOD_PKB_1 | 255 | 263 | PF00069 | 0.510 |
MOD_Plk_1 | 34 | 40 | PF00069 | 0.469 |
MOD_Plk_1 | 393 | 399 | PF00069 | 0.653 |
MOD_Plk_1 | 57 | 63 | PF00069 | 0.450 |
MOD_Plk_1 | 637 | 643 | PF00069 | 0.536 |
MOD_Plk_1 | 713 | 719 | PF00069 | 0.645 |
MOD_Plk_2-3 | 139 | 145 | PF00069 | 0.677 |
MOD_Plk_2-3 | 26 | 32 | PF00069 | 0.510 |
MOD_Plk_2-3 | 34 | 40 | PF00069 | 0.523 |
MOD_Plk_4 | 599 | 605 | PF00069 | 0.532 |
MOD_ProDKin_1 | 111 | 117 | PF00069 | 0.753 |
MOD_ProDKin_1 | 187 | 193 | PF00069 | 0.773 |
MOD_ProDKin_1 | 223 | 229 | PF00069 | 0.701 |
MOD_ProDKin_1 | 278 | 284 | PF00069 | 0.509 |
MOD_ProDKin_1 | 367 | 373 | PF00069 | 0.530 |
MOD_ProDKin_1 | 492 | 498 | PF00069 | 0.582 |
MOD_SUMO_for_1 | 121 | 124 | PF00179 | 0.492 |
MOD_SUMO_rev_2 | 40 | 50 | PF00179 | 0.507 |
MOD_SUMO_rev_2 | 584 | 594 | PF00179 | 0.688 |
TRG_DiLeu_BaLyEn_6 | 348 | 353 | PF01217 | 0.474 |
TRG_ENDOCYTIC_2 | 38 | 41 | PF00928 | 0.451 |
TRG_ENDOCYTIC_2 | 432 | 435 | PF00928 | 0.691 |
TRG_ENDOCYTIC_2 | 676 | 679 | PF00928 | 0.556 |
TRG_ER_diArg_1 | 254 | 257 | PF00400 | 0.510 |
TRG_ER_diArg_1 | 335 | 337 | PF00400 | 0.514 |
TRG_ER_diArg_1 | 445 | 447 | PF00400 | 0.721 |
TRG_ER_diArg_1 | 478 | 481 | PF00400 | 0.547 |
TRG_ER_diArg_1 | 528 | 531 | PF00400 | 0.608 |
TRG_ER_diArg_1 | 585 | 587 | PF00400 | 0.608 |
TRG_ER_diArg_1 | 8 | 11 | PF00400 | 0.486 |
TRG_ER_diArg_1 | 88 | 90 | PF00400 | 0.373 |
TRG_Pf-PMV_PEXEL_1 | 42 | 46 | PF00026 | 0.512 |
TRG_Pf-PMV_PEXEL_1 | 580 | 584 | PF00026 | 0.536 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDF9 | Leptomonas seymouri | 69% | 100% |
A0A3S7X9C0 | Leishmania donovani | 91% | 100% |
A4HMT2 | Leishmania braziliensis | 81% | 100% |
A4IBD0 | Leishmania infantum | 91% | 100% |
C9ZZ89 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
E9AF86 | Leishmania major | 90% | 100% |