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: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0031974 | membrane-enclosed lumen | 2 | 1 |
GO:0031981 | nuclear lumen | 5 | 1 |
GO:0032838 | plasma membrane bounded cell projection cytoplasm | 4 | 1 |
GO:0043233 | organelle lumen | 3 | 1 |
GO:0070013 | intracellular organelle lumen | 4 | 1 |
GO:0097014 | ciliary plasm | 5 | 1 |
GO:0099568 | cytoplasmic region | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HLX6
Term | Name | Level | Count |
---|---|---|---|
GO:0006807 | nitrogen compound metabolic process | 2 | 3 |
GO:0008152 | metabolic process | 1 | 3 |
GO:0019538 | protein metabolic process | 3 | 3 |
GO:0032446 | protein modification by small protein conjugation | 6 | 3 |
GO:0036211 | protein modification process | 4 | 3 |
GO:0043170 | macromolecule metabolic process | 3 | 3 |
GO:0043412 | macromolecule modification | 4 | 3 |
GO:0044238 | primary metabolic process | 2 | 3 |
GO:0045116 | protein neddylation | 7 | 3 |
GO:0070647 | protein modification by small protein conjugation or removal | 5 | 3 |
GO:0071704 | organic substance metabolic process | 2 | 3 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 3 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 9 |
GO:0008641 | ubiquitin-like modifier activating enzyme activity | 2 | 9 |
GO:0016874 | ligase activity | 2 | 9 |
GO:0016877 | ligase activity, forming carbon-sulfur bonds | 3 | 9 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 9 |
GO:0140657 | ATP-dependent activity | 1 | 9 |
GO:0019781 | NEDD8 activating enzyme activity | 3 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 177 | 181 | PF00656 | 0.405 |
CLV_C14_Caspase3-7 | 294 | 298 | PF00656 | 0.458 |
CLV_C14_Caspase3-7 | 737 | 741 | PF00656 | 0.410 |
CLV_NRD_NRD_1 | 316 | 318 | PF00675 | 0.409 |
CLV_NRD_NRD_1 | 358 | 360 | PF00675 | 0.458 |
CLV_NRD_NRD_1 | 625 | 627 | PF00675 | 0.327 |
CLV_NRD_NRD_1 | 645 | 647 | PF00675 | 0.409 |
CLV_NRD_NRD_1 | 662 | 664 | PF00675 | 0.482 |
CLV_PCSK_KEX2_1 | 316 | 318 | PF00082 | 0.409 |
CLV_PCSK_KEX2_1 | 358 | 360 | PF00082 | 0.442 |
CLV_PCSK_KEX2_1 | 625 | 627 | PF00082 | 0.317 |
CLV_PCSK_KEX2_1 | 645 | 647 | PF00082 | 0.409 |
CLV_PCSK_KEX2_1 | 662 | 664 | PF00082 | 0.482 |
CLV_PCSK_SKI1_1 | 21 | 25 | PF00082 | 0.521 |
CLV_PCSK_SKI1_1 | 251 | 255 | PF00082 | 0.266 |
CLV_PCSK_SKI1_1 | 404 | 408 | PF00082 | 0.376 |
CLV_PCSK_SKI1_1 | 585 | 589 | PF00082 | 0.460 |
CLV_PCSK_SKI1_1 | 67 | 71 | PF00082 | 0.399 |
CLV_PCSK_SKI1_1 | 692 | 696 | PF00082 | 0.537 |
CLV_PCSK_SKI1_1 | 723 | 727 | PF00082 | 0.385 |
CLV_PCSK_SKI1_1 | 786 | 790 | PF00082 | 0.263 |
CLV_Separin_Metazoa | 392 | 396 | PF03568 | 0.330 |
DEG_MDM2_SWIB_1 | 315 | 322 | PF02201 | 0.432 |
DOC_CKS1_1 | 87 | 92 | PF01111 | 0.281 |
DOC_CYCLIN_RxL_1 | 56 | 64 | PF00134 | 0.241 |
DOC_CYCLIN_RxL_1 | 582 | 593 | PF00134 | 0.447 |
DOC_CYCLIN_yCln2_LP_2 | 418 | 424 | PF00134 | 0.316 |
DOC_MAPK_DCC_7 | 225 | 235 | PF00069 | 0.415 |
DOC_MAPK_gen_1 | 21 | 31 | PF00069 | 0.355 |
DOC_MAPK_gen_1 | 622 | 630 | PF00069 | 0.245 |
DOC_MAPK_MEF2A_6 | 225 | 234 | PF00069 | 0.390 |
DOC_MAPK_MEF2A_6 | 765 | 772 | PF00069 | 0.427 |
DOC_PP1_RVXF_1 | 601 | 608 | PF00149 | 0.431 |
DOC_PP1_RVXF_1 | 623 | 630 | PF00149 | 0.416 |
DOC_PP4_FxxP_1 | 571 | 574 | PF00568 | 0.501 |
DOC_PP4_FxxP_1 | 87 | 90 | PF00568 | 0.245 |
DOC_USP7_MATH_1 | 292 | 296 | PF00917 | 0.434 |
DOC_USP7_MATH_1 | 348 | 352 | PF00917 | 0.466 |
DOC_USP7_MATH_1 | 408 | 412 | PF00917 | 0.467 |
DOC_USP7_MATH_1 | 57 | 61 | PF00917 | 0.453 |
DOC_USP7_MATH_1 | 610 | 614 | PF00917 | 0.325 |
DOC_USP7_UBL2_3 | 373 | 377 | PF12436 | 0.484 |
DOC_WW_Pin1_4 | 117 | 122 | PF00397 | 0.332 |
DOC_WW_Pin1_4 | 210 | 215 | PF00397 | 0.375 |
DOC_WW_Pin1_4 | 411 | 416 | PF00397 | 0.451 |
DOC_WW_Pin1_4 | 417 | 422 | PF00397 | 0.405 |
DOC_WW_Pin1_4 | 467 | 472 | PF00397 | 0.500 |
DOC_WW_Pin1_4 | 575 | 580 | PF00397 | 0.336 |
DOC_WW_Pin1_4 | 86 | 91 | PF00397 | 0.369 |
DOC_WW_Pin1_4 | 92 | 97 | PF00397 | 0.355 |
LIG_14-3-3_CanoR_1 | 145 | 150 | PF00244 | 0.502 |
LIG_14-3-3_CanoR_1 | 347 | 353 | PF00244 | 0.481 |
LIG_14-3-3_CanoR_1 | 612 | 619 | PF00244 | 0.533 |
LIG_14-3-3_CanoR_1 | 632 | 637 | PF00244 | 0.451 |
LIG_14-3-3_CanoR_1 | 67 | 72 | PF00244 | 0.399 |
LIG_14-3-3_CanoR_1 | 723 | 732 | PF00244 | 0.281 |
LIG_Actin_WH2_2 | 379 | 397 | PF00022 | 0.435 |
LIG_Actin_WH2_2 | 577 | 592 | PF00022 | 0.278 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.651 |
LIG_BRCT_BRCA1_1 | 181 | 185 | PF00533 | 0.670 |
LIG_BRCT_BRCA1_1 | 335 | 339 | PF00533 | 0.532 |
LIG_deltaCOP1_diTrp_1 | 597 | 607 | PF00928 | 0.384 |
LIG_Dynein_DLC8_1 | 151 | 157 | PF01221 | 0.470 |
LIG_FHA_1 | 10 | 16 | PF00498 | 0.580 |
LIG_FHA_1 | 127 | 133 | PF00498 | 0.308 |
LIG_FHA_1 | 161 | 167 | PF00498 | 0.527 |
LIG_FHA_1 | 221 | 227 | PF00498 | 0.481 |
LIG_FHA_1 | 336 | 342 | PF00498 | 0.443 |
LIG_FHA_1 | 373 | 379 | PF00498 | 0.480 |
LIG_FHA_1 | 40 | 46 | PF00498 | 0.393 |
LIG_FHA_1 | 451 | 457 | PF00498 | 0.433 |
LIG_FHA_1 | 49 | 55 | PF00498 | 0.384 |
LIG_FHA_1 | 490 | 496 | PF00498 | 0.612 |
LIG_FHA_1 | 515 | 521 | PF00498 | 0.459 |
LIG_FHA_1 | 590 | 596 | PF00498 | 0.323 |
LIG_FHA_1 | 629 | 635 | PF00498 | 0.420 |
LIG_FHA_1 | 66 | 72 | PF00498 | 0.424 |
LIG_FHA_1 | 753 | 759 | PF00498 | 0.374 |
LIG_FHA_1 | 782 | 788 | PF00498 | 0.424 |
LIG_FHA_2 | 153 | 159 | PF00498 | 0.459 |
LIG_FHA_2 | 340 | 346 | PF00498 | 0.381 |
LIG_FHA_2 | 541 | 547 | PF00498 | 0.390 |
LIG_FHA_2 | 592 | 598 | PF00498 | 0.257 |
LIG_FHA_2 | 613 | 619 | PF00498 | 0.359 |
LIG_FHA_2 | 68 | 74 | PF00498 | 0.296 |
LIG_FHA_2 | 726 | 732 | PF00498 | 0.409 |
LIG_LIR_Apic_2 | 84 | 90 | PF02991 | 0.186 |
LIG_LIR_Gen_1 | 631 | 638 | PF02991 | 0.557 |
LIG_LIR_Nem_3 | 206 | 212 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 271 | 276 | PF02991 | 0.416 |
LIG_LIR_Nem_3 | 303 | 307 | PF02991 | 0.356 |
LIG_LIR_Nem_3 | 343 | 349 | PF02991 | 0.389 |
LIG_LIR_Nem_3 | 519 | 525 | PF02991 | 0.336 |
LIG_LIR_Nem_3 | 631 | 636 | PF02991 | 0.535 |
LIG_LYPXL_yS_3 | 307 | 310 | PF13949 | 0.377 |
LIG_NRBOX | 389 | 395 | PF00104 | 0.442 |
LIG_PDZ_Class_2 | 785 | 790 | PF00595 | 0.444 |
LIG_Pex14_1 | 124 | 128 | PF04695 | 0.348 |
LIG_Pex14_1 | 629 | 633 | PF04695 | 0.262 |
LIG_Pex14_2 | 315 | 319 | PF04695 | 0.410 |
LIG_Pex14_2 | 636 | 640 | PF04695 | 0.387 |
LIG_Pex14_2 | 650 | 654 | PF04695 | 0.245 |
LIG_PTB_Apo_2 | 782 | 789 | PF02174 | 0.444 |
LIG_SH2_CRK | 346 | 350 | PF00017 | 0.429 |
LIG_SH2_CRK | 504 | 508 | PF00017 | 0.404 |
LIG_SH2_GRB2like | 783 | 786 | PF00017 | 0.454 |
LIG_SH2_STAP1 | 128 | 132 | PF00017 | 0.305 |
LIG_SH2_STAP1 | 491 | 495 | PF00017 | 0.404 |
LIG_SH2_STAP1 | 783 | 787 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 128 | 131 | PF00017 | 0.311 |
LIG_SH2_STAT5 | 247 | 250 | PF00017 | 0.445 |
LIG_SH2_STAT5 | 304 | 307 | PF00017 | 0.321 |
LIG_SH2_STAT5 | 491 | 494 | PF00017 | 0.420 |
LIG_SH2_STAT5 | 511 | 514 | PF00017 | 0.317 |
LIG_SH2_STAT5 | 633 | 636 | PF00017 | 0.340 |
LIG_SH2_STAT5 | 783 | 786 | PF00017 | 0.454 |
LIG_SH2_STAT5 | 86 | 89 | PF00017 | 0.461 |
LIG_SH3_1 | 225 | 231 | PF00018 | 0.433 |
LIG_SH3_3 | 156 | 162 | PF00018 | 0.506 |
LIG_SH3_3 | 194 | 200 | PF00018 | 0.380 |
LIG_SH3_3 | 211 | 217 | PF00018 | 0.425 |
LIG_SH3_3 | 225 | 231 | PF00018 | 0.445 |
LIG_SH3_3 | 253 | 259 | PF00018 | 0.536 |
LIG_SH3_3 | 493 | 499 | PF00018 | 0.458 |
LIG_SH3_3 | 90 | 96 | PF00018 | 0.231 |
LIG_SUMO_SIM_anti_2 | 201 | 207 | PF11976 | 0.330 |
LIG_SUMO_SIM_anti_2 | 543 | 549 | PF11976 | 0.238 |
LIG_SUMO_SIM_anti_2 | 68 | 74 | PF11976 | 0.344 |
LIG_SUMO_SIM_par_1 | 174 | 182 | PF11976 | 0.399 |
LIG_SUMO_SIM_par_1 | 201 | 207 | PF11976 | 0.337 |
LIG_SUMO_SIM_par_1 | 231 | 238 | PF11976 | 0.404 |
LIG_SUMO_SIM_par_1 | 50 | 56 | PF11976 | 0.387 |
LIG_SUMO_SIM_par_1 | 67 | 74 | PF11976 | 0.181 |
LIG_TRAF2_1 | 116 | 119 | PF00917 | 0.344 |
LIG_TRAF2_1 | 323 | 326 | PF00917 | 0.513 |
LIG_TRAF2_1 | 362 | 365 | PF00917 | 0.385 |
LIG_TRAF2_1 | 656 | 659 | PF00917 | 0.397 |
LIG_TRAF2_1 | 728 | 731 | PF00917 | 0.447 |
LIG_TRAF2_1 | 759 | 762 | PF00917 | 0.314 |
LIG_TYR_ITIM | 305 | 310 | PF00017 | 0.301 |
LIG_TYR_ITIM | 520 | 525 | PF00017 | 0.425 |
LIG_UBA3_1 | 576 | 585 | PF00899 | 0.301 |
LIG_WRC_WIRS_1 | 349 | 354 | PF05994 | 0.263 |
LIG_WRC_WIRS_1 | 633 | 638 | PF05994 | 0.346 |
MOD_CDK_SPK_2 | 117 | 122 | PF00069 | 0.283 |
MOD_CDK_SPxxK_3 | 467 | 474 | PF00069 | 0.503 |
MOD_CK1_1 | 181 | 187 | PF00069 | 0.729 |
MOD_CK1_1 | 198 | 204 | PF00069 | 0.490 |
MOD_CK1_1 | 213 | 219 | PF00069 | 0.299 |
MOD_CK1_1 | 221 | 227 | PF00069 | 0.366 |
MOD_CK1_1 | 333 | 339 | PF00069 | 0.560 |
MOD_CK1_1 | 411 | 417 | PF00069 | 0.446 |
MOD_CK1_1 | 467 | 473 | PF00069 | 0.500 |
MOD_CK1_1 | 476 | 482 | PF00069 | 0.479 |
MOD_CK1_1 | 670 | 676 | PF00069 | 0.491 |
MOD_CK1_1 | 686 | 692 | PF00069 | 0.395 |
MOD_CK1_1 | 711 | 717 | PF00069 | 0.338 |
MOD_CK2_1 | 117 | 123 | PF00069 | 0.253 |
MOD_CK2_1 | 152 | 158 | PF00069 | 0.465 |
MOD_CK2_1 | 476 | 482 | PF00069 | 0.577 |
MOD_CK2_1 | 540 | 546 | PF00069 | 0.229 |
MOD_CK2_1 | 591 | 597 | PF00069 | 0.259 |
MOD_CK2_1 | 610 | 616 | PF00069 | 0.274 |
MOD_CK2_1 | 653 | 659 | PF00069 | 0.337 |
MOD_CK2_1 | 725 | 731 | PF00069 | 0.408 |
MOD_Cter_Amidation | 623 | 626 | PF01082 | 0.244 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.744 |
MOD_GlcNHglycan | 112 | 115 | PF01048 | 0.312 |
MOD_GlcNHglycan | 163 | 166 | PF01048 | 0.473 |
MOD_GlcNHglycan | 180 | 184 | PF01048 | 0.709 |
MOD_GlcNHglycan | 237 | 240 | PF01048 | 0.387 |
MOD_GlcNHglycan | 294 | 297 | PF01048 | 0.437 |
MOD_GlcNHglycan | 478 | 481 | PF01048 | 0.552 |
MOD_GlcNHglycan | 508 | 511 | PF01048 | 0.401 |
MOD_GlcNHglycan | 607 | 610 | PF01048 | 0.485 |
MOD_GlcNHglycan | 639 | 643 | PF01048 | 0.332 |
MOD_GlcNHglycan | 669 | 672 | PF01048 | 0.570 |
MOD_GlcNHglycan | 77 | 80 | PF01048 | 0.271 |
MOD_GSK3_1 | 179 | 186 | PF00069 | 0.616 |
MOD_GSK3_1 | 191 | 198 | PF00069 | 0.593 |
MOD_GSK3_1 | 326 | 333 | PF00069 | 0.588 |
MOD_GSK3_1 | 335 | 342 | PF00069 | 0.449 |
MOD_GSK3_1 | 469 | 476 | PF00069 | 0.603 |
MOD_GSK3_1 | 57 | 64 | PF00069 | 0.359 |
MOD_GSK3_1 | 575 | 582 | PF00069 | 0.345 |
MOD_GSK3_1 | 628 | 635 | PF00069 | 0.506 |
MOD_GSK3_1 | 686 | 693 | PF00069 | 0.460 |
MOD_GSK3_1 | 747 | 754 | PF00069 | 0.453 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.361 |
MOD_N-GLC_1 | 186 | 191 | PF02516 | 0.583 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.592 |
MOD_NEK2_1 | 10 | 15 | PF00069 | 0.522 |
MOD_NEK2_1 | 185 | 190 | PF00069 | 0.585 |
MOD_NEK2_1 | 218 | 223 | PF00069 | 0.445 |
MOD_NEK2_1 | 234 | 239 | PF00069 | 0.402 |
MOD_NEK2_1 | 243 | 248 | PF00069 | 0.405 |
MOD_NEK2_1 | 450 | 455 | PF00069 | 0.347 |
MOD_NEK2_1 | 48 | 53 | PF00069 | 0.295 |
MOD_NEK2_1 | 515 | 520 | PF00069 | 0.367 |
MOD_NEK2_1 | 61 | 66 | PF00069 | 0.309 |
MOD_NEK2_1 | 672 | 677 | PF00069 | 0.529 |
MOD_NEK2_1 | 708 | 713 | PF00069 | 0.632 |
MOD_NEK2_1 | 97 | 102 | PF00069 | 0.293 |
MOD_PIKK_1 | 152 | 158 | PF00454 | 0.465 |
MOD_PIKK_1 | 257 | 263 | PF00454 | 0.538 |
MOD_PIKK_1 | 683 | 689 | PF00454 | 0.572 |
MOD_PIKK_1 | 718 | 724 | PF00454 | 0.371 |
MOD_PKA_2 | 152 | 158 | PF00069 | 0.674 |
MOD_PKA_2 | 235 | 241 | PF00069 | 0.396 |
MOD_PKA_2 | 473 | 479 | PF00069 | 0.510 |
MOD_PKA_2 | 605 | 611 | PF00069 | 0.304 |
MOD_PKA_2 | 733 | 739 | PF00069 | 0.360 |
MOD_Plk_1 | 10 | 16 | PF00069 | 0.458 |
MOD_Plk_1 | 708 | 714 | PF00069 | 0.537 |
MOD_Plk_4 | 198 | 204 | PF00069 | 0.347 |
MOD_Plk_4 | 300 | 306 | PF00069 | 0.497 |
MOD_Plk_4 | 348 | 354 | PF00069 | 0.469 |
MOD_Plk_4 | 516 | 522 | PF00069 | 0.424 |
MOD_Plk_4 | 57 | 63 | PF00069 | 0.323 |
MOD_Plk_4 | 591 | 597 | PF00069 | 0.348 |
MOD_Plk_4 | 67 | 73 | PF00069 | 0.282 |
MOD_Plk_4 | 711 | 717 | PF00069 | 0.338 |
MOD_Plk_4 | 97 | 103 | PF00069 | 0.344 |
MOD_ProDKin_1 | 117 | 123 | PF00069 | 0.332 |
MOD_ProDKin_1 | 210 | 216 | PF00069 | 0.369 |
MOD_ProDKin_1 | 411 | 417 | PF00069 | 0.446 |
MOD_ProDKin_1 | 467 | 473 | PF00069 | 0.500 |
MOD_ProDKin_1 | 575 | 581 | PF00069 | 0.324 |
MOD_ProDKin_1 | 86 | 92 | PF00069 | 0.369 |
MOD_SUMO_rev_2 | 324 | 329 | PF00179 | 0.499 |
TRG_DiLeu_BaEn_1 | 680 | 685 | PF01217 | 0.419 |
TRG_DiLeu_BaEn_1 | 762 | 767 | PF01217 | 0.310 |
TRG_DiLeu_BaLyEn_6 | 165 | 170 | PF01217 | 0.258 |
TRG_DiLeu_BaLyEn_6 | 214 | 219 | PF01217 | 0.440 |
TRG_DiLeu_BaLyEn_6 | 583 | 588 | PF01217 | 0.442 |
TRG_ENDOCYTIC_2 | 173 | 176 | PF00928 | 0.539 |
TRG_ENDOCYTIC_2 | 209 | 212 | PF00928 | 0.430 |
TRG_ENDOCYTIC_2 | 307 | 310 | PF00928 | 0.319 |
TRG_ENDOCYTIC_2 | 346 | 349 | PF00928 | 0.337 |
TRG_ENDOCYTIC_2 | 522 | 525 | PF00928 | 0.332 |
TRG_ENDOCYTIC_2 | 633 | 636 | PF00928 | 0.511 |
TRG_ER_diArg_1 | 315 | 317 | PF00400 | 0.397 |
TRG_ER_diArg_1 | 357 | 359 | PF00400 | 0.391 |
TRG_ER_diArg_1 | 619 | 622 | PF00400 | 0.431 |
TRG_ER_diArg_1 | 625 | 627 | PF00400 | 0.416 |
TRG_ER_diArg_1 | 768 | 771 | PF00400 | 0.306 |
TRG_Pf-PMV_PEXEL_1 | 523 | 527 | PF00026 | 0.351 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5J2 | Leptomonas seymouri | 49% | 100% |
A0A0S4JRQ2 | Bodo saltans | 22% | 96% |
A0A3R7MGL1 | Trypanosoma rangeli | 27% | 100% |
A0A3S7X724 | Leishmania donovani | 71% | 99% |
A4I9A5 | Leishmania infantum | 71% | 99% |
E9B4A5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 73% | 100% |
Q4Q3S1 | Leishmania major | 72% | 99% |
Q5ZIE6 | Gallus gallus | 24% | 100% |
V5AV29 | Trypanosoma cruzi | 27% | 100% |