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: 11 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: A4IC64
Term | Name | Level | Count |
---|---|---|---|
GO:0001522 | pseudouridine synthesis | 6 | 12 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009451 | RNA modification | 5 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016070 | RNA metabolic process | 5 | 12 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0043412 | macromolecule modification | 4 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0046483 | heterocycle metabolic process | 3 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0090304 | nucleic acid metabolic process | 4 | 12 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
GO:0000154 | rRNA modification | 6 | 1 |
GO:0000455 | enzyme-directed rRNA pseudouridine synthesis | 8 | 1 |
GO:0006364 | rRNA processing | 8 | 1 |
GO:0006396 | RNA processing | 6 | 1 |
GO:0016072 | rRNA metabolic process | 7 | 1 |
GO:0031118 | rRNA pseudouridine synthesis | 7 | 1 |
GO:0034470 | ncRNA processing | 7 | 1 |
GO:0034660 | ncRNA metabolic process | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003723 | RNA binding | 4 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0009982 | pseudouridine synthase activity | 4 | 12 |
GO:0016853 | isomerase activity | 2 | 12 |
GO:0016866 | intramolecular transferase activity | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
GO:0009055 | electron transfer activity | 3 | 1 |
GO:0016491 | oxidoreductase activity | 2 | 1 |
GO:0020037 | heme binding | 4 | 1 |
GO:0043167 | ion binding | 2 | 1 |
GO:0043169 | cation binding | 3 | 1 |
GO:0046872 | metal ion binding | 4 | 1 |
GO:0046906 | tetrapyrrole binding | 3 | 1 |
GO:0106029 | tRNA pseudouridine synthase activity | 5 | 1 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 1 |
GO:0140101 | catalytic activity, acting on a tRNA | 4 | 1 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 235 | 239 | PF00656 | 0.539 |
CLV_C14_Caspase3-7 | 443 | 447 | PF00656 | 0.412 |
CLV_C14_Caspase3-7 | 631 | 635 | PF00656 | 0.441 |
CLV_NRD_NRD_1 | 12 | 14 | PF00675 | 0.438 |
CLV_NRD_NRD_1 | 128 | 130 | PF00675 | 0.381 |
CLV_NRD_NRD_1 | 249 | 251 | PF00675 | 0.545 |
CLV_NRD_NRD_1 | 331 | 333 | PF00675 | 0.415 |
CLV_NRD_NRD_1 | 336 | 338 | PF00675 | 0.431 |
CLV_NRD_NRD_1 | 671 | 673 | PF00675 | 0.231 |
CLV_NRD_NRD_1 | 729 | 731 | PF00675 | 0.388 |
CLV_PCSK_FUR_1 | 247 | 251 | PF00082 | 0.411 |
CLV_PCSK_FUR_1 | 329 | 333 | PF00082 | 0.456 |
CLV_PCSK_KEX2_1 | 128 | 130 | PF00082 | 0.373 |
CLV_PCSK_KEX2_1 | 249 | 251 | PF00082 | 0.432 |
CLV_PCSK_KEX2_1 | 331 | 333 | PF00082 | 0.412 |
CLV_PCSK_KEX2_1 | 336 | 338 | PF00082 | 0.427 |
CLV_PCSK_KEX2_1 | 387 | 389 | PF00082 | 0.351 |
CLV_PCSK_KEX2_1 | 671 | 673 | PF00082 | 0.236 |
CLV_PCSK_KEX2_1 | 729 | 731 | PF00082 | 0.423 |
CLV_PCSK_PC1ET2_1 | 387 | 389 | PF00082 | 0.351 |
CLV_PCSK_PC7_1 | 332 | 338 | PF00082 | 0.433 |
CLV_PCSK_SKI1_1 | 101 | 105 | PF00082 | 0.530 |
CLV_PCSK_SKI1_1 | 13 | 17 | PF00082 | 0.512 |
CLV_PCSK_SKI1_1 | 283 | 287 | PF00082 | 0.424 |
CLV_PCSK_SKI1_1 | 357 | 361 | PF00082 | 0.428 |
CLV_PCSK_SKI1_1 | 465 | 469 | PF00082 | 0.302 |
CLV_PCSK_SKI1_1 | 564 | 568 | PF00082 | 0.236 |
CLV_PCSK_SKI1_1 | 60 | 64 | PF00082 | 0.489 |
CLV_PCSK_SKI1_1 | 699 | 703 | PF00082 | 0.262 |
DEG_APCC_DBOX_1 | 12 | 20 | PF00400 | 0.485 |
DEG_APCC_DBOX_1 | 33 | 41 | PF00400 | 0.448 |
DEG_APCC_DBOX_1 | 437 | 445 | PF00400 | 0.375 |
DEG_APCC_DBOX_1 | 464 | 472 | PF00400 | 0.332 |
DEG_APCC_DBOX_1 | 728 | 736 | PF00400 | 0.458 |
DEG_SCF_FBW7_1 | 78 | 84 | PF00400 | 0.474 |
DEG_SPOP_SBC_1 | 82 | 86 | PF00917 | 0.551 |
DEG_SPOP_SBC_1 | 89 | 93 | PF00917 | 0.553 |
DOC_CDC14_PxL_1 | 509 | 517 | PF14671 | 0.472 |
DOC_CKS1_1 | 213 | 218 | PF01111 | 0.400 |
DOC_CKS1_1 | 542 | 547 | PF01111 | 0.415 |
DOC_CKS1_1 | 78 | 83 | PF01111 | 0.460 |
DOC_CYCLIN_RxL_1 | 460 | 469 | PF00134 | 0.308 |
DOC_CYCLIN_RxL_1 | 727 | 738 | PF00134 | 0.325 |
DOC_CYCLIN_yCln2_LP_2 | 213 | 219 | PF00134 | 0.375 |
DOC_MAPK_gen_1 | 641 | 649 | PF00069 | 0.466 |
DOC_MAPK_MEF2A_6 | 610 | 619 | PF00069 | 0.519 |
DOC_MAPK_RevD_3 | 323 | 337 | PF00069 | 0.530 |
DOC_PP1_RVXF_1 | 643 | 650 | PF00149 | 0.424 |
DOC_PP1_RVXF_1 | 652 | 658 | PF00149 | 0.424 |
DOC_PP4_FxxP_1 | 289 | 292 | PF00568 | 0.249 |
DOC_PP4_FxxP_1 | 310 | 313 | PF00568 | 0.474 |
DOC_PP4_FxxP_1 | 709 | 712 | PF00568 | 0.340 |
DOC_USP7_MATH_1 | 201 | 205 | PF00917 | 0.484 |
DOC_USP7_MATH_1 | 206 | 210 | PF00917 | 0.444 |
DOC_USP7_MATH_1 | 236 | 240 | PF00917 | 0.398 |
DOC_USP7_MATH_1 | 262 | 266 | PF00917 | 0.650 |
DOC_USP7_MATH_1 | 339 | 343 | PF00917 | 0.566 |
DOC_USP7_MATH_1 | 359 | 363 | PF00917 | 0.398 |
DOC_USP7_MATH_1 | 459 | 463 | PF00917 | 0.324 |
DOC_USP7_MATH_1 | 577 | 581 | PF00917 | 0.437 |
DOC_USP7_MATH_1 | 591 | 595 | PF00917 | 0.394 |
DOC_USP7_MATH_1 | 89 | 93 | PF00917 | 0.741 |
DOC_WW_Pin1_4 | 157 | 162 | PF00397 | 0.509 |
DOC_WW_Pin1_4 | 212 | 217 | PF00397 | 0.407 |
DOC_WW_Pin1_4 | 309 | 314 | PF00397 | 0.483 |
DOC_WW_Pin1_4 | 406 | 411 | PF00397 | 0.468 |
DOC_WW_Pin1_4 | 541 | 546 | PF00397 | 0.552 |
DOC_WW_Pin1_4 | 60 | 65 | PF00397 | 0.523 |
DOC_WW_Pin1_4 | 77 | 82 | PF00397 | 0.426 |
LIG_14-3-3_CanoR_1 | 140 | 146 | PF00244 | 0.376 |
LIG_14-3-3_CanoR_1 | 22 | 28 | PF00244 | 0.458 |
LIG_14-3-3_CanoR_1 | 261 | 269 | PF00244 | 0.579 |
LIG_14-3-3_CanoR_1 | 394 | 400 | PF00244 | 0.541 |
LIG_14-3-3_CanoR_1 | 438 | 448 | PF00244 | 0.546 |
LIG_14-3-3_CanoR_1 | 44 | 50 | PF00244 | 0.548 |
LIG_14-3-3_CanoR_1 | 477 | 482 | PF00244 | 0.533 |
LIG_14-3-3_CanoR_1 | 534 | 542 | PF00244 | 0.424 |
LIG_14-3-3_CanoR_1 | 729 | 735 | PF00244 | 0.313 |
LIG_Actin_RPEL_3 | 37 | 56 | PF02755 | 0.380 |
LIG_Actin_WH2_2 | 341 | 359 | PF00022 | 0.499 |
LIG_Actin_WH2_2 | 608 | 626 | PF00022 | 0.462 |
LIG_APCC_ABBA_1 | 626 | 631 | PF00400 | 0.441 |
LIG_BRCT_BRCA1_1 | 601 | 605 | PF00533 | 0.519 |
LIG_BRCT_BRCA1_1 | 705 | 709 | PF00533 | 0.432 |
LIG_deltaCOP1_diTrp_1 | 352 | 358 | PF00928 | 0.512 |
LIG_EH1_1 | 1 | 9 | PF00400 | 0.413 |
LIG_EH1_1 | 275 | 283 | PF00400 | 0.429 |
LIG_FHA_1 | 22 | 28 | PF00498 | 0.454 |
LIG_FHA_1 | 544 | 550 | PF00498 | 0.428 |
LIG_FHA_1 | 554 | 560 | PF00498 | 0.416 |
LIG_FHA_2 | 120 | 126 | PF00498 | 0.395 |
LIG_FHA_2 | 345 | 351 | PF00498 | 0.376 |
LIG_FHA_2 | 464 | 470 | PF00498 | 0.419 |
LIG_FHA_2 | 501 | 507 | PF00498 | 0.413 |
LIG_FHA_2 | 91 | 97 | PF00498 | 0.552 |
LIG_GBD_Chelix_1 | 244 | 252 | PF00786 | 0.353 |
LIG_Integrin_RGD_1 | 370 | 372 | PF01839 | 0.371 |
LIG_Integrin_RGD_1 | 405 | 407 | PF01839 | 0.475 |
LIG_LIR_Apic_2 | 286 | 292 | PF02991 | 0.257 |
LIG_LIR_Apic_2 | 706 | 712 | PF02991 | 0.345 |
LIG_LIR_Gen_1 | 352 | 360 | PF02991 | 0.511 |
LIG_LIR_Gen_1 | 609 | 619 | PF02991 | 0.436 |
LIG_LIR_LC3C_4 | 519 | 524 | PF02991 | 0.369 |
LIG_LIR_Nem_3 | 352 | 358 | PF02991 | 0.512 |
LIG_LIR_Nem_3 | 412 | 418 | PF02991 | 0.309 |
LIG_LIR_Nem_3 | 462 | 467 | PF02991 | 0.294 |
LIG_LIR_Nem_3 | 609 | 615 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 642 | 647 | PF02991 | 0.416 |
LIG_Pex14_1 | 306 | 310 | PF04695 | 0.355 |
LIG_Pex14_2 | 222 | 226 | PF04695 | 0.356 |
LIG_SH2_CRK | 612 | 616 | PF00017 | 0.453 |
LIG_SH2_CRK | 644 | 648 | PF00017 | 0.424 |
LIG_SH2_STAP1 | 399 | 403 | PF00017 | 0.299 |
LIG_SH2_STAT5 | 114 | 117 | PF00017 | 0.526 |
LIG_SH2_STAT5 | 374 | 377 | PF00017 | 0.517 |
LIG_SH2_STAT5 | 418 | 421 | PF00017 | 0.479 |
LIG_SH3_3 | 191 | 197 | PF00018 | 0.479 |
LIG_SH3_3 | 291 | 297 | PF00018 | 0.406 |
LIG_SH3_3 | 487 | 493 | PF00018 | 0.317 |
LIG_SH3_3 | 504 | 510 | PF00018 | 0.346 |
LIG_SH3_3 | 521 | 527 | PF00018 | 0.492 |
LIG_SH3_3 | 615 | 621 | PF00018 | 0.453 |
LIG_SUMO_SIM_anti_2 | 517 | 525 | PF11976 | 0.279 |
LIG_SUMO_SIM_anti_2 | 546 | 554 | PF11976 | 0.439 |
LIG_SUMO_SIM_par_1 | 517 | 525 | PF11976 | 0.400 |
LIG_TYR_ITSM | 640 | 647 | PF00017 | 0.273 |
LIG_UBA3_1 | 55 | 60 | PF00899 | 0.407 |
LIG_WRC_WIRS_1 | 223 | 228 | PF05994 | 0.427 |
MOD_CK1_1 | 195 | 201 | PF00069 | 0.355 |
MOD_CK1_1 | 232 | 238 | PF00069 | 0.454 |
MOD_CK1_1 | 239 | 245 | PF00069 | 0.386 |
MOD_CK1_1 | 257 | 263 | PF00069 | 0.593 |
MOD_CK1_1 | 344 | 350 | PF00069 | 0.467 |
MOD_CK1_1 | 606 | 612 | PF00069 | 0.268 |
MOD_CK1_1 | 695 | 701 | PF00069 | 0.423 |
MOD_CK2_1 | 119 | 125 | PF00069 | 0.370 |
MOD_CK2_1 | 346 | 352 | PF00069 | 0.358 |
MOD_CK2_1 | 500 | 506 | PF00069 | 0.416 |
MOD_CK2_1 | 735 | 741 | PF00069 | 0.361 |
MOD_Cter_Amidation | 11 | 14 | PF01082 | 0.525 |
MOD_Cter_Amidation | 664 | 667 | PF01082 | 0.242 |
MOD_GlcNHglycan | 199 | 202 | PF01048 | 0.352 |
MOD_GlcNHglycan | 203 | 206 | PF01048 | 0.333 |
MOD_GlcNHglycan | 230 | 234 | PF01048 | 0.452 |
MOD_GlcNHglycan | 265 | 268 | PF01048 | 0.625 |
MOD_GlcNHglycan | 361 | 365 | PF01048 | 0.509 |
MOD_GlcNHglycan | 375 | 378 | PF01048 | 0.390 |
MOD_GlcNHglycan | 578 | 582 | PF01048 | 0.252 |
MOD_GlcNHglycan | 601 | 604 | PF01048 | 0.242 |
MOD_GlcNHglycan | 85 | 88 | PF01048 | 0.624 |
MOD_GSK3_1 | 175 | 182 | PF00069 | 0.450 |
MOD_GSK3_1 | 197 | 204 | PF00069 | 0.338 |
MOD_GSK3_1 | 232 | 239 | PF00069 | 0.523 |
MOD_GSK3_1 | 428 | 435 | PF00069 | 0.496 |
MOD_GSK3_1 | 459 | 466 | PF00069 | 0.313 |
MOD_GSK3_1 | 477 | 484 | PF00069 | 0.391 |
MOD_GSK3_1 | 537 | 544 | PF00069 | 0.303 |
MOD_GSK3_1 | 599 | 606 | PF00069 | 0.266 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.466 |
MOD_N-GLC_1 | 257 | 262 | PF02516 | 0.643 |
MOD_NEK2_1 | 175 | 180 | PF00069 | 0.412 |
MOD_NEK2_1 | 222 | 227 | PF00069 | 0.437 |
MOD_NEK2_1 | 360 | 365 | PF00069 | 0.535 |
MOD_NEK2_1 | 395 | 400 | PF00069 | 0.333 |
MOD_NEK2_1 | 411 | 416 | PF00069 | 0.470 |
MOD_NEK2_1 | 439 | 444 | PF00069 | 0.356 |
MOD_NEK2_1 | 471 | 476 | PF00069 | 0.362 |
MOD_NEK2_1 | 530 | 535 | PF00069 | 0.256 |
MOD_NEK2_1 | 537 | 542 | PF00069 | 0.226 |
MOD_NEK2_1 | 599 | 604 | PF00069 | 0.233 |
MOD_NEK2_1 | 735 | 740 | PF00069 | 0.431 |
MOD_NEK2_2 | 591 | 596 | PF00069 | 0.242 |
MOD_PIKK_1 | 239 | 245 | PF00454 | 0.350 |
MOD_PIKK_1 | 537 | 543 | PF00454 | 0.242 |
MOD_PIKK_1 | 62 | 68 | PF00454 | 0.296 |
MOD_PKA_2 | 21 | 27 | PF00069 | 0.455 |
MOD_PKA_2 | 432 | 438 | PF00069 | 0.484 |
MOD_PKA_2 | 476 | 482 | PF00069 | 0.582 |
MOD_PKA_2 | 735 | 741 | PF00069 | 0.397 |
MOD_PKB_1 | 138 | 146 | PF00069 | 0.344 |
MOD_Plk_1 | 283 | 289 | PF00069 | 0.390 |
MOD_Plk_1 | 411 | 417 | PF00069 | 0.466 |
MOD_Plk_4 | 206 | 212 | PF00069 | 0.366 |
MOD_Plk_4 | 341 | 347 | PF00069 | 0.469 |
MOD_Plk_4 | 370 | 376 | PF00069 | 0.551 |
MOD_Plk_4 | 432 | 438 | PF00069 | 0.413 |
MOD_Plk_4 | 45 | 51 | PF00069 | 0.502 |
MOD_Plk_4 | 459 | 465 | PF00069 | 0.322 |
MOD_Plk_4 | 54 | 60 | PF00069 | 0.328 |
MOD_Plk_4 | 692 | 698 | PF00069 | 0.422 |
MOD_Plk_4 | 705 | 711 | PF00069 | 0.261 |
MOD_Plk_4 | 730 | 736 | PF00069 | 0.474 |
MOD_ProDKin_1 | 157 | 163 | PF00069 | 0.511 |
MOD_ProDKin_1 | 212 | 218 | PF00069 | 0.403 |
MOD_ProDKin_1 | 309 | 315 | PF00069 | 0.478 |
MOD_ProDKin_1 | 406 | 412 | PF00069 | 0.470 |
MOD_ProDKin_1 | 541 | 547 | PF00069 | 0.435 |
MOD_ProDKin_1 | 60 | 66 | PF00069 | 0.522 |
MOD_ProDKin_1 | 77 | 83 | PF00069 | 0.442 |
MOD_SUMO_for_1 | 115 | 118 | PF00179 | 0.394 |
MOD_SUMO_for_1 | 486 | 489 | PF00179 | 0.346 |
MOD_SUMO_rev_2 | 479 | 488 | PF00179 | 0.523 |
MOD_SUMO_rev_2 | 631 | 640 | PF00179 | 0.268 |
TRG_DiLeu_BaLyEn_6 | 391 | 396 | PF01217 | 0.337 |
TRG_DiLeu_BaLyEn_6 | 446 | 451 | PF01217 | 0.509 |
TRG_ENDOCYTIC_2 | 172 | 175 | PF00928 | 0.311 |
TRG_ENDOCYTIC_2 | 612 | 615 | PF00928 | 0.242 |
TRG_ENDOCYTIC_2 | 644 | 647 | PF00928 | 0.251 |
TRG_ER_diArg_1 | 137 | 140 | PF00400 | 0.392 |
TRG_ER_diArg_1 | 246 | 249 | PF00400 | 0.375 |
TRG_ER_diArg_1 | 328 | 331 | PF00400 | 0.426 |
TRG_ER_diArg_1 | 335 | 337 | PF00400 | 0.426 |
TRG_ER_diArg_1 | 640 | 643 | PF00400 | 0.463 |
TRG_ER_diArg_1 | 670 | 672 | PF00400 | 0.265 |
TRG_ER_diArg_1 | 728 | 730 | PF00400 | 0.440 |
TRG_Pf-PMV_PEXEL_1 | 388 | 392 | PF00026 | 0.339 |
TRG_Pf-PMV_PEXEL_1 | 452 | 456 | PF00026 | 0.416 |
TRG_Pf-PMV_PEXEL_1 | 465 | 469 | PF00026 | 0.281 |
TRG_Pf-PMV_PEXEL_1 | 69 | 73 | PF00026 | 0.370 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1F5 | Leptomonas seymouri | 62% | 100% |
A0A0S4JPK1 | Bodo saltans | 37% | 100% |
A0A1X0NY31 | Trypanosomatidae | 44% | 97% |
A0A3Q8IN41 | Leishmania donovani | 99% | 100% |
A0A422P4N9 | Trypanosoma rangeli | 46% | 100% |
A4HNH3 | Leishmania braziliensis | 82% | 100% |
C9ZKA6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 46% | 89% |
E9AFY4 | Leishmania major | 94% | 100% |
E9B737 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
V5B2G2 | Trypanosoma cruzi | 45% | 100% |