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: 2 |
NetGPI | no | yes: 0, no: 2 |
Related structures:
AlphaFold database: A4H589
Term | Name | Level | Count |
---|---|---|---|
GO:0006807 | nitrogen compound metabolic process | 2 | 3 |
GO:0008152 | metabolic process | 1 | 3 |
GO:0016925 | protein sumoylation | 7 | 3 |
GO:0018193 | peptidyl-amino acid modification | 5 | 3 |
GO:0018205 | peptidyl-lysine modification | 6 | 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: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:0000166 | nucleotide binding | 3 | 3 |
GO:0003824 | catalytic activity | 1 | 3 |
GO:0005488 | binding | 1 | 3 |
GO:0005524 | ATP binding | 5 | 3 |
GO:0008641 | ubiquitin-like modifier activating enzyme activity | 2 | 3 |
GO:0016874 | ligase activity | 2 | 3 |
GO:0016877 | ligase activity, forming carbon-sulfur bonds | 3 | 3 |
GO:0017076 | purine nucleotide binding | 4 | 3 |
GO:0019948 | SUMO activating enzyme activity | 3 | 3 |
GO:0030554 | adenyl nucleotide binding | 5 | 3 |
GO:0032553 | ribonucleotide binding | 3 | 3 |
GO:0032555 | purine ribonucleotide binding | 4 | 3 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 3 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 3 |
GO:0036094 | small molecule binding | 2 | 3 |
GO:0043167 | ion binding | 2 | 3 |
GO:0043168 | anion binding | 3 | 3 |
GO:0097159 | organic cyclic compound binding | 2 | 3 |
GO:0097367 | carbohydrate derivative binding | 2 | 3 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 3 |
GO:0140657 | ATP-dependent activity | 1 | 3 |
GO:1901265 | nucleoside phosphate binding | 3 | 3 |
GO:1901363 | heterocyclic compound binding | 2 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 183 | 187 | PF00656 | 0.494 |
CLV_C14_Caspase3-7 | 298 | 302 | PF00656 | 0.199 |
CLV_C14_Caspase3-7 | 469 | 473 | PF00656 | 0.477 |
CLV_NRD_NRD_1 | 325 | 327 | PF00675 | 0.258 |
CLV_NRD_NRD_1 | 349 | 351 | PF00675 | 0.326 |
CLV_NRD_NRD_1 | 78 | 80 | PF00675 | 0.447 |
CLV_PCSK_FUR_1 | 347 | 351 | PF00082 | 0.326 |
CLV_PCSK_KEX2_1 | 325 | 327 | PF00082 | 0.300 |
CLV_PCSK_KEX2_1 | 349 | 351 | PF00082 | 0.326 |
CLV_PCSK_KEX2_1 | 43 | 45 | PF00082 | 0.666 |
CLV_PCSK_KEX2_1 | 78 | 80 | PF00082 | 0.682 |
CLV_PCSK_PC1ET2_1 | 43 | 45 | PF00082 | 0.666 |
CLV_PCSK_SKI1_1 | 266 | 270 | PF00082 | 0.199 |
CLV_PCSK_SKI1_1 | 287 | 291 | PF00082 | 0.208 |
CLV_PCSK_SKI1_1 | 307 | 311 | PF00082 | 0.150 |
CLV_PCSK_SKI1_1 | 320 | 324 | PF00082 | 0.199 |
CLV_PCSK_SKI1_1 | 326 | 330 | PF00082 | 0.199 |
CLV_PCSK_SKI1_1 | 527 | 531 | PF00082 | 0.383 |
CLV_PCSK_SKI1_1 | 566 | 570 | PF00082 | 0.278 |
DEG_APCC_DBOX_1 | 306 | 314 | PF00400 | 0.208 |
DEG_COP1_1 | 178 | 187 | PF00400 | 0.504 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.495 |
DEG_SCF_TRCP1_1 | 550 | 556 | PF00400 | 0.441 |
DOC_CYCLIN_RxL_1 | 279 | 290 | PF00134 | 0.208 |
DOC_CYCLIN_yCln2_LP_2 | 264 | 270 | PF00134 | 0.208 |
DOC_MAPK_RevD_3 | 311 | 326 | PF00069 | 0.208 |
DOC_PP1_RVXF_1 | 564 | 570 | PF00149 | 0.277 |
DOC_PP2B_LxvP_1 | 208 | 211 | PF13499 | 0.433 |
DOC_USP7_MATH_1 | 144 | 148 | PF00917 | 0.546 |
DOC_USP7_MATH_1 | 177 | 181 | PF00917 | 0.516 |
DOC_USP7_MATH_1 | 21 | 25 | PF00917 | 0.461 |
DOC_USP7_MATH_1 | 28 | 32 | PF00917 | 0.469 |
DOC_USP7_MATH_1 | 478 | 482 | PF00917 | 0.508 |
DOC_USP7_MATH_1 | 493 | 497 | PF00917 | 0.475 |
DOC_USP7_MATH_1 | 506 | 510 | PF00917 | 0.446 |
DOC_USP7_MATH_1 | 590 | 594 | PF00917 | 0.367 |
DOC_USP7_MATH_1 | 81 | 85 | PF00917 | 0.465 |
DOC_USP7_MATH_1 | 98 | 102 | PF00917 | 0.437 |
DOC_WW_Pin1_4 | 128 | 133 | PF00397 | 0.497 |
DOC_WW_Pin1_4 | 164 | 169 | PF00397 | 0.629 |
DOC_WW_Pin1_4 | 241 | 246 | PF00397 | 0.493 |
DOC_WW_Pin1_4 | 336 | 341 | PF00397 | 0.208 |
DOC_WW_Pin1_4 | 348 | 353 | PF00397 | 0.209 |
DOC_WW_Pin1_4 | 464 | 469 | PF00397 | 0.208 |
DOC_WW_Pin1_4 | 584 | 589 | PF00397 | 0.369 |
DOC_WW_Pin1_4 | 94 | 99 | PF00397 | 0.517 |
LIG_14-3-3_CanoR_1 | 239 | 245 | PF00244 | 0.442 |
LIG_14-3-3_CanoR_1 | 248 | 253 | PF00244 | 0.414 |
LIG_14-3-3_CanoR_1 | 287 | 295 | PF00244 | 0.208 |
LIG_14-3-3_CanoR_1 | 445 | 450 | PF00244 | 0.199 |
LIG_14-3-3_CanoR_1 | 518 | 528 | PF00244 | 0.326 |
LIG_BIR_III_2 | 186 | 190 | PF00653 | 0.572 |
LIG_BRCT_BRCA1_1 | 155 | 159 | PF00533 | 0.387 |
LIG_Clathr_ClatBox_1 | 294 | 298 | PF01394 | 0.208 |
LIG_FHA_1 | 193 | 199 | PF00498 | 0.392 |
LIG_FHA_1 | 231 | 237 | PF00498 | 0.605 |
LIG_FHA_1 | 341 | 347 | PF00498 | 0.208 |
LIG_FHA_1 | 434 | 440 | PF00498 | 0.199 |
LIG_FHA_1 | 445 | 451 | PF00498 | 0.199 |
LIG_FHA_1 | 58 | 64 | PF00498 | 0.472 |
LIG_FHA_2 | 111 | 117 | PF00498 | 0.450 |
LIG_FHA_2 | 169 | 175 | PF00498 | 0.502 |
LIG_FHA_2 | 181 | 187 | PF00498 | 0.479 |
LIG_FHA_2 | 213 | 219 | PF00498 | 0.442 |
LIG_FHA_2 | 86 | 92 | PF00498 | 0.498 |
LIG_GBD_Chelix_1 | 560 | 568 | PF00786 | 0.286 |
LIG_LIR_Gen_1 | 149 | 160 | PF02991 | 0.517 |
LIG_LIR_Gen_1 | 458 | 468 | PF02991 | 0.199 |
LIG_LIR_Nem_3 | 149 | 155 | PF02991 | 0.535 |
LIG_LIR_Nem_3 | 156 | 160 | PF02991 | 0.344 |
LIG_LIR_Nem_3 | 369 | 375 | PF02991 | 0.313 |
LIG_LIR_Nem_3 | 420 | 425 | PF02991 | 0.295 |
LIG_LIR_Nem_3 | 458 | 463 | PF02991 | 0.199 |
LIG_MAD2 | 197 | 205 | PF02301 | 0.382 |
LIG_NRBOX | 563 | 569 | PF00104 | 0.285 |
LIG_PCNA_yPIPBox_3 | 415 | 428 | PF02747 | 0.208 |
LIG_PDZ_Class_2 | 593 | 598 | PF00595 | 0.412 |
LIG_Pex14_2 | 371 | 375 | PF04695 | 0.317 |
LIG_SH2_NCK_1 | 367 | 371 | PF00017 | 0.199 |
LIG_SH2_NCK_1 | 80 | 84 | PF00017 | 0.460 |
LIG_SH2_SRC | 367 | 370 | PF00017 | 0.199 |
LIG_SH2_STAP1 | 367 | 371 | PF00017 | 0.199 |
LIG_SH2_STAP1 | 455 | 459 | PF00017 | 0.199 |
LIG_SH2_STAP1 | 460 | 464 | PF00017 | 0.199 |
LIG_SH2_STAT3 | 410 | 413 | PF00017 | 0.199 |
LIG_SH2_STAT5 | 516 | 519 | PF00017 | 0.330 |
LIG_SH3_3 | 15 | 21 | PF00018 | 0.594 |
LIG_SH3_3 | 160 | 166 | PF00018 | 0.457 |
LIG_SH3_3 | 179 | 185 | PF00018 | 0.452 |
LIG_SH3_3 | 30 | 36 | PF00018 | 0.620 |
LIG_SH3_3 | 334 | 340 | PF00018 | 0.208 |
LIG_SH3_3 | 426 | 432 | PF00018 | 0.214 |
LIG_SUMO_SIM_par_1 | 293 | 299 | PF11976 | 0.208 |
LIG_SUMO_SIM_par_1 | 574 | 581 | PF11976 | 0.335 |
LIG_TRAF2_1 | 495 | 498 | PF00917 | 0.508 |
LIG_UBA3_1 | 576 | 580 | PF00899 | 0.334 |
LIG_WRC_WIRS_1 | 579 | 584 | PF05994 | 0.379 |
MOD_CDC14_SPxK_1 | 131 | 134 | PF00782 | 0.511 |
MOD_CDK_SPxK_1 | 128 | 134 | PF00069 | 0.501 |
MOD_CDK_SPxxK_3 | 241 | 248 | PF00069 | 0.451 |
MOD_CK1_1 | 102 | 108 | PF00069 | 0.461 |
MOD_CK1_1 | 117 | 123 | PF00069 | 0.418 |
MOD_CK1_1 | 142 | 148 | PF00069 | 0.510 |
MOD_CK1_1 | 153 | 159 | PF00069 | 0.329 |
MOD_CK1_1 | 180 | 186 | PF00069 | 0.559 |
MOD_CK1_1 | 24 | 30 | PF00069 | 0.503 |
MOD_CK1_1 | 241 | 247 | PF00069 | 0.574 |
MOD_CK1_1 | 466 | 472 | PF00069 | 0.208 |
MOD_CK1_1 | 481 | 487 | PF00069 | 0.461 |
MOD_CK1_1 | 492 | 498 | PF00069 | 0.488 |
MOD_CK1_1 | 533 | 539 | PF00069 | 0.457 |
MOD_CK1_1 | 54 | 60 | PF00069 | 0.554 |
MOD_CK1_1 | 553 | 559 | PF00069 | 0.315 |
MOD_CK1_1 | 578 | 584 | PF00069 | 0.365 |
MOD_CK2_1 | 110 | 116 | PF00069 | 0.445 |
MOD_CK2_1 | 168 | 174 | PF00069 | 0.501 |
MOD_CK2_1 | 175 | 181 | PF00069 | 0.498 |
MOD_CK2_1 | 212 | 218 | PF00069 | 0.440 |
MOD_CK2_1 | 492 | 498 | PF00069 | 0.516 |
MOD_CK2_1 | 85 | 91 | PF00069 | 0.494 |
MOD_Cter_Amidation | 347 | 350 | PF01082 | 0.208 |
MOD_GlcNHglycan | 116 | 119 | PF01048 | 0.586 |
MOD_GlcNHglycan | 148 | 151 | PF01048 | 0.505 |
MOD_GlcNHglycan | 152 | 155 | PF01048 | 0.480 |
MOD_GlcNHglycan | 224 | 227 | PF01048 | 0.688 |
MOD_GlcNHglycan | 228 | 231 | PF01048 | 0.575 |
MOD_GlcNHglycan | 23 | 26 | PF01048 | 0.512 |
MOD_GlcNHglycan | 30 | 33 | PF01048 | 0.465 |
MOD_GlcNHglycan | 385 | 388 | PF01048 | 0.215 |
MOD_GlcNHglycan | 404 | 407 | PF01048 | 0.199 |
MOD_GlcNHglycan | 491 | 494 | PF01048 | 0.528 |
MOD_GlcNHglycan | 532 | 535 | PF01048 | 0.449 |
MOD_GlcNHglycan | 550 | 553 | PF01048 | 0.423 |
MOD_GlcNHglycan | 555 | 558 | PF01048 | 0.335 |
MOD_GlcNHglycan | 592 | 595 | PF01048 | 0.393 |
MOD_GlcNHglycan | 6 | 9 | PF01048 | 0.453 |
MOD_GlcNHglycan | 88 | 91 | PF01048 | 0.767 |
MOD_GSK3_1 | 110 | 117 | PF00069 | 0.392 |
MOD_GSK3_1 | 142 | 149 | PF00069 | 0.508 |
MOD_GSK3_1 | 164 | 171 | PF00069 | 0.479 |
MOD_GSK3_1 | 222 | 229 | PF00069 | 0.633 |
MOD_GSK3_1 | 24 | 31 | PF00069 | 0.475 |
MOD_GSK3_1 | 244 | 251 | PF00069 | 0.582 |
MOD_GSK3_1 | 296 | 303 | PF00069 | 0.288 |
MOD_GSK3_1 | 316 | 323 | PF00069 | 0.241 |
MOD_GSK3_1 | 332 | 339 | PF00069 | 0.199 |
MOD_GSK3_1 | 459 | 466 | PF00069 | 0.208 |
MOD_GSK3_1 | 478 | 485 | PF00069 | 0.453 |
MOD_GSK3_1 | 489 | 496 | PF00069 | 0.491 |
MOD_GSK3_1 | 51 | 58 | PF00069 | 0.480 |
MOD_GSK3_1 | 512 | 519 | PF00069 | 0.351 |
MOD_GSK3_1 | 548 | 555 | PF00069 | 0.471 |
MOD_GSK3_1 | 81 | 88 | PF00069 | 0.492 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.468 |
MOD_LATS_1 | 443 | 449 | PF00433 | 0.199 |
MOD_N-GLC_1 | 114 | 119 | PF02516 | 0.432 |
MOD_N-GLC_1 | 383 | 388 | PF02516 | 0.199 |
MOD_NEK2_1 | 332 | 337 | PF00069 | 0.199 |
MOD_NEK2_1 | 402 | 407 | PF00069 | 0.199 |
MOD_NEK2_1 | 459 | 464 | PF00069 | 0.208 |
MOD_NEK2_1 | 479 | 484 | PF00069 | 0.448 |
MOD_NEK2_1 | 85 | 90 | PF00069 | 0.571 |
MOD_NEK2_2 | 358 | 363 | PF00069 | 0.208 |
MOD_NEK2_2 | 438 | 443 | PF00069 | 0.199 |
MOD_NEK2_2 | 575 | 580 | PF00069 | 0.337 |
MOD_PIKK_1 | 287 | 293 | PF00454 | 0.208 |
MOD_PIKK_1 | 493 | 499 | PF00454 | 0.515 |
MOD_PIKK_1 | 55 | 61 | PF00454 | 0.475 |
MOD_PKA_2 | 212 | 218 | PF00069 | 0.551 |
MOD_PKA_2 | 238 | 244 | PF00069 | 0.555 |
MOD_PKA_2 | 444 | 450 | PF00069 | 0.199 |
MOD_PKA_2 | 482 | 488 | PF00069 | 0.506 |
MOD_PKB_1 | 44 | 52 | PF00069 | 0.504 |
MOD_PKB_1 | 525 | 533 | PF00069 | 0.389 |
MOD_Plk_1 | 180 | 186 | PF00069 | 0.504 |
MOD_Plk_1 | 191 | 197 | PF00069 | 0.368 |
MOD_Plk_1 | 512 | 518 | PF00069 | 0.353 |
MOD_Plk_2-3 | 296 | 302 | PF00069 | 0.199 |
MOD_Plk_4 | 117 | 123 | PF00069 | 0.446 |
MOD_Plk_4 | 254 | 260 | PF00069 | 0.544 |
MOD_Plk_4 | 445 | 451 | PF00069 | 0.199 |
MOD_Plk_4 | 459 | 465 | PF00069 | 0.199 |
MOD_Plk_4 | 512 | 518 | PF00069 | 0.353 |
MOD_Plk_4 | 536 | 542 | PF00069 | 0.460 |
MOD_Plk_4 | 578 | 584 | PF00069 | 0.440 |
MOD_ProDKin_1 | 128 | 134 | PF00069 | 0.501 |
MOD_ProDKin_1 | 164 | 170 | PF00069 | 0.632 |
MOD_ProDKin_1 | 241 | 247 | PF00069 | 0.495 |
MOD_ProDKin_1 | 336 | 342 | PF00069 | 0.208 |
MOD_ProDKin_1 | 348 | 354 | PF00069 | 0.209 |
MOD_ProDKin_1 | 464 | 470 | PF00069 | 0.208 |
MOD_ProDKin_1 | 584 | 590 | PF00069 | 0.363 |
MOD_ProDKin_1 | 94 | 100 | PF00069 | 0.512 |
MOD_SUMO_rev_2 | 466 | 476 | PF00179 | 0.476 |
TRG_DiLeu_BaLyEn_6 | 398 | 403 | PF01217 | 0.199 |
TRG_DiLeu_BaLyEn_6 | 563 | 568 | PF01217 | 0.283 |
TRG_ENDOCYTIC_2 | 372 | 375 | PF00928 | 0.208 |
TRG_ENDOCYTIC_2 | 460 | 463 | PF00928 | 0.199 |
TRG_ER_diArg_1 | 325 | 327 | PF00400 | 0.313 |
TRG_ER_diArg_1 | 346 | 349 | PF00400 | 0.352 |
TRG_ER_diArg_1 | 44 | 47 | PF00400 | 0.508 |
TRG_ER_diArg_1 | 524 | 527 | PF00400 | 0.341 |
TRG_ER_diArg_1 | 77 | 79 | PF00400 | 0.442 |
TRG_NLS_MonoExtC_3 | 42 | 48 | PF00514 | 0.667 |
TRG_NLS_MonoExtN_4 | 40 | 47 | PF00514 | 0.502 |
TRG_Pf-PMV_PEXEL_1 | 457 | 461 | PF00026 | 0.199 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
V5BH49 | Trypanosoma cruzi | 39% | 100% |