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: 1, no: 8 |
NetGPI | no | yes: 0, no: 9 |
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: E9B3C1
Term | Name | Level | Count |
---|---|---|---|
GO:0001522 | pseudouridine synthesis | 6 | 10 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 10 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 10 |
GO:0006807 | nitrogen compound metabolic process | 2 | 10 |
GO:0008152 | metabolic process | 1 | 10 |
GO:0009451 | RNA modification | 5 | 10 |
GO:0009987 | cellular process | 1 | 10 |
GO:0016070 | RNA metabolic process | 5 | 10 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 10 |
GO:0043170 | macromolecule metabolic process | 3 | 10 |
GO:0043412 | macromolecule modification | 4 | 10 |
GO:0044237 | cellular metabolic process | 2 | 10 |
GO:0044238 | primary metabolic process | 2 | 10 |
GO:0046483 | heterocycle metabolic process | 3 | 10 |
GO:0071704 | organic substance metabolic process | 2 | 10 |
GO:0090304 | nucleic acid metabolic process | 4 | 10 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 10 |
GO:0003723 | RNA binding | 4 | 10 |
GO:0003824 | catalytic activity | 1 | 10 |
GO:0005488 | binding | 1 | 10 |
GO:0009982 | pseudouridine synthase activity | 4 | 10 |
GO:0016853 | isomerase activity | 2 | 10 |
GO:0016866 | intramolecular transferase activity | 3 | 10 |
GO:0097159 | organic cyclic compound binding | 2 | 10 |
GO:1901363 | heterocyclic compound binding | 2 | 10 |
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 |
GO:0016829 | lyase activity | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 177 | 181 | PF00656 | 0.640 |
CLV_NRD_NRD_1 | 123 | 125 | PF00675 | 0.642 |
CLV_NRD_NRD_1 | 148 | 150 | PF00675 | 0.419 |
CLV_NRD_NRD_1 | 156 | 158 | PF00675 | 0.426 |
CLV_NRD_NRD_1 | 205 | 207 | PF00675 | 0.666 |
CLV_NRD_NRD_1 | 239 | 241 | PF00675 | 0.285 |
CLV_NRD_NRD_1 | 357 | 359 | PF00675 | 0.299 |
CLV_NRD_NRD_1 | 389 | 391 | PF00675 | 0.343 |
CLV_NRD_NRD_1 | 638 | 640 | PF00675 | 0.441 |
CLV_NRD_NRD_1 | 673 | 675 | PF00675 | 0.551 |
CLV_NRD_NRD_1 | 84 | 86 | PF00675 | 0.392 |
CLV_PCSK_KEX2_1 | 123 | 125 | PF00082 | 0.644 |
CLV_PCSK_KEX2_1 | 148 | 150 | PF00082 | 0.419 |
CLV_PCSK_KEX2_1 | 156 | 158 | PF00082 | 0.426 |
CLV_PCSK_KEX2_1 | 205 | 207 | PF00082 | 0.666 |
CLV_PCSK_KEX2_1 | 241 | 243 | PF00082 | 0.260 |
CLV_PCSK_KEX2_1 | 357 | 359 | PF00082 | 0.343 |
CLV_PCSK_KEX2_1 | 389 | 391 | PF00082 | 0.343 |
CLV_PCSK_KEX2_1 | 638 | 640 | PF00082 | 0.563 |
CLV_PCSK_KEX2_1 | 672 | 674 | PF00082 | 0.625 |
CLV_PCSK_PC1ET2_1 | 241 | 243 | PF00082 | 0.260 |
CLV_PCSK_PC7_1 | 668 | 674 | PF00082 | 0.383 |
CLV_PCSK_SKI1_1 | 250 | 254 | PF00082 | 0.318 |
CLV_PCSK_SKI1_1 | 295 | 299 | PF00082 | 0.356 |
CLV_PCSK_SKI1_1 | 384 | 388 | PF00082 | 0.461 |
CLV_PCSK_SKI1_1 | 433 | 437 | PF00082 | 0.175 |
CLV_PCSK_SKI1_1 | 500 | 504 | PF00082 | 0.322 |
CLV_PCSK_SKI1_1 | 710 | 714 | PF00082 | 0.333 |
CLV_PCSK_SKI1_1 | 85 | 89 | PF00082 | 0.501 |
CLV_Separin_Metazoa | 153 | 157 | PF03568 | 0.483 |
DEG_APCC_DBOX_1 | 80 | 88 | PF00400 | 0.490 |
DEG_MDM2_SWIB_1 | 424 | 432 | PF02201 | 0.377 |
DOC_ANK_TNKS_1 | 122 | 129 | PF00023 | 0.477 |
DOC_ANK_TNKS_1 | 175 | 182 | PF00023 | 0.616 |
DOC_CYCLIN_RxL_1 | 292 | 300 | PF00134 | 0.372 |
DOC_CYCLIN_yCln2_LP_2 | 309 | 315 | PF00134 | 0.366 |
DOC_MAPK_gen_1 | 167 | 175 | PF00069 | 0.321 |
DOC_MAPK_gen_1 | 270 | 277 | PF00069 | 0.332 |
DOC_MAPK_gen_1 | 638 | 645 | PF00069 | 0.372 |
DOC_MAPK_MEF2A_6 | 690 | 697 | PF00069 | 0.352 |
DOC_MAPK_NFAT4_5 | 690 | 698 | PF00069 | 0.281 |
DOC_MAPK_RevD_3 | 190 | 206 | PF00069 | 0.463 |
DOC_PP1_RVXF_1 | 345 | 352 | PF00149 | 0.377 |
DOC_PP1_RVXF_1 | 623 | 630 | PF00149 | 0.443 |
DOC_PP4_FxxP_1 | 697 | 700 | PF00568 | 0.302 |
DOC_USP7_MATH_1 | 127 | 131 | PF00917 | 0.654 |
DOC_USP7_MATH_1 | 135 | 139 | PF00917 | 0.636 |
DOC_USP7_MATH_1 | 140 | 144 | PF00917 | 0.646 |
DOC_USP7_MATH_1 | 191 | 195 | PF00917 | 0.603 |
DOC_USP7_MATH_1 | 315 | 319 | PF00917 | 0.375 |
DOC_USP7_MATH_1 | 325 | 329 | PF00917 | 0.370 |
DOC_USP7_MATH_1 | 431 | 435 | PF00917 | 0.286 |
DOC_USP7_MATH_1 | 456 | 460 | PF00917 | 0.157 |
DOC_USP7_MATH_1 | 481 | 485 | PF00917 | 0.377 |
DOC_USP7_MATH_1 | 517 | 521 | PF00917 | 0.329 |
DOC_USP7_MATH_1 | 555 | 559 | PF00917 | 0.733 |
DOC_WW_Pin1_4 | 18 | 23 | PF00397 | 0.574 |
DOC_WW_Pin1_4 | 216 | 221 | PF00397 | 0.719 |
DOC_WW_Pin1_4 | 26 | 31 | PF00397 | 0.516 |
DOC_WW_Pin1_4 | 359 | 364 | PF00397 | 0.324 |
LIG_14-3-3_CanoR_1 | 170 | 174 | PF00244 | 0.353 |
LIG_14-3-3_CanoR_1 | 193 | 202 | PF00244 | 0.721 |
LIG_14-3-3_CanoR_1 | 279 | 283 | PF00244 | 0.266 |
LIG_14-3-3_CanoR_1 | 295 | 304 | PF00244 | 0.390 |
LIG_14-3-3_CanoR_1 | 324 | 334 | PF00244 | 0.423 |
LIG_14-3-3_CanoR_1 | 407 | 415 | PF00244 | 0.317 |
LIG_14-3-3_CanoR_1 | 470 | 474 | PF00244 | 0.240 |
LIG_14-3-3_CanoR_1 | 62 | 66 | PF00244 | 0.505 |
LIG_14-3-3_CanoR_1 | 628 | 635 | PF00244 | 0.467 |
LIG_14-3-3_CanoR_1 | 71 | 77 | PF00244 | 0.597 |
LIG_BIR_III_2 | 217 | 221 | PF00653 | 0.610 |
LIG_BRCT_BRCA1_1 | 519 | 523 | PF00533 | 0.260 |
LIG_deltaCOP1_diTrp_1 | 626 | 635 | PF00928 | 0.420 |
LIG_FHA_1 | 221 | 227 | PF00498 | 0.616 |
LIG_FHA_1 | 464 | 470 | PF00498 | 0.380 |
LIG_FHA_1 | 501 | 507 | PF00498 | 0.444 |
LIG_FHA_1 | 690 | 696 | PF00498 | 0.494 |
LIG_FHA_1 | 704 | 710 | PF00498 | 0.299 |
LIG_FHA_2 | 111 | 117 | PF00498 | 0.512 |
LIG_FHA_2 | 132 | 138 | PF00498 | 0.497 |
LIG_FHA_2 | 175 | 181 | PF00498 | 0.666 |
LIG_FHA_2 | 205 | 211 | PF00498 | 0.745 |
LIG_FHA_2 | 363 | 369 | PF00498 | 0.391 |
LIG_LIR_Apic_2 | 696 | 700 | PF02991 | 0.418 |
LIG_LIR_Gen_1 | 113 | 122 | PF02991 | 0.517 |
LIG_LIR_Gen_1 | 318 | 327 | PF02991 | 0.266 |
LIG_LIR_Gen_1 | 42 | 52 | PF02991 | 0.369 |
LIG_LIR_Gen_1 | 491 | 502 | PF02991 | 0.312 |
LIG_LIR_Gen_1 | 701 | 712 | PF02991 | 0.308 |
LIG_LIR_Nem_3 | 113 | 118 | PF02991 | 0.491 |
LIG_LIR_Nem_3 | 255 | 259 | PF02991 | 0.347 |
LIG_LIR_Nem_3 | 318 | 322 | PF02991 | 0.249 |
LIG_LIR_Nem_3 | 338 | 344 | PF02991 | 0.372 |
LIG_LIR_Nem_3 | 396 | 402 | PF02991 | 0.281 |
LIG_LIR_Nem_3 | 42 | 48 | PF02991 | 0.414 |
LIG_LIR_Nem_3 | 472 | 476 | PF02991 | 0.369 |
LIG_LIR_Nem_3 | 491 | 497 | PF02991 | 0.312 |
LIG_LIR_Nem_3 | 520 | 525 | PF02991 | 0.323 |
LIG_LIR_Nem_3 | 648 | 652 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 701 | 707 | PF02991 | 0.315 |
LIG_LIR_Nem_3 | 93 | 99 | PF02991 | 0.508 |
LIG_LYPXL_S_1 | 158 | 162 | PF13949 | 0.492 |
LIG_LYPXL_yS_3 | 159 | 162 | PF13949 | 0.368 |
LIG_MLH1_MIPbox_1 | 519 | 523 | PF16413 | 0.377 |
LIG_Pex14_2 | 399 | 403 | PF04695 | 0.260 |
LIG_Pex14_2 | 424 | 428 | PF04695 | 0.370 |
LIG_SH2_CRK | 319 | 323 | PF00017 | 0.377 |
LIG_SH2_CRK | 704 | 708 | PF00017 | 0.295 |
LIG_SH2_NCK_1 | 704 | 708 | PF00017 | 0.295 |
LIG_SH2_PTP2 | 234 | 237 | PF00017 | 0.332 |
LIG_SH2_SRC | 234 | 237 | PF00017 | 0.332 |
LIG_SH2_STAP1 | 319 | 323 | PF00017 | 0.377 |
LIG_SH2_STAP1 | 704 | 708 | PF00017 | 0.295 |
LIG_SH2_STAT3 | 402 | 405 | PF00017 | 0.260 |
LIG_SH2_STAT5 | 234 | 237 | PF00017 | 0.461 |
LIG_SH2_STAT5 | 256 | 259 | PF00017 | 0.320 |
LIG_SH2_STAT5 | 402 | 405 | PF00017 | 0.260 |
LIG_SH2_STAT5 | 45 | 48 | PF00017 | 0.392 |
LIG_SH2_STAT5 | 476 | 479 | PF00017 | 0.380 |
LIG_SH2_STAT5 | 509 | 512 | PF00017 | 0.377 |
LIG_SH2_STAT5 | 529 | 532 | PF00017 | 0.448 |
LIG_SH3_3 | 16 | 22 | PF00018 | 0.681 |
LIG_SH3_3 | 309 | 315 | PF00018 | 0.269 |
LIG_SH3_3 | 569 | 575 | PF00018 | 0.473 |
LIG_SH3_3 | 640 | 646 | PF00018 | 0.372 |
LIG_SH3_3 | 650 | 656 | PF00018 | 0.323 |
MOD_CDK_SPK_2 | 18 | 23 | PF00069 | 0.527 |
MOD_CK1_1 | 114 | 120 | PF00069 | 0.623 |
MOD_CK1_1 | 194 | 200 | PF00069 | 0.579 |
MOD_CK1_1 | 219 | 225 | PF00069 | 0.675 |
MOD_CK1_1 | 326 | 332 | PF00069 | 0.342 |
MOD_CK1_1 | 35 | 41 | PF00069 | 0.635 |
MOD_CK1_1 | 362 | 368 | PF00069 | 0.286 |
MOD_CK1_1 | 547 | 553 | PF00069 | 0.548 |
MOD_CK1_1 | 557 | 563 | PF00069 | 0.568 |
MOD_CK1_1 | 564 | 570 | PF00069 | 0.714 |
MOD_CK1_1 | 90 | 96 | PF00069 | 0.604 |
MOD_CK2_1 | 114 | 120 | PF00069 | 0.520 |
MOD_CK2_1 | 131 | 137 | PF00069 | 0.440 |
MOD_CK2_1 | 204 | 210 | PF00069 | 0.730 |
MOD_CK2_1 | 362 | 368 | PF00069 | 0.394 |
MOD_CK2_1 | 564 | 570 | PF00069 | 0.598 |
MOD_CMANNOS | 612 | 615 | PF00535 | 0.456 |
MOD_GlcNHglycan | 129 | 132 | PF01048 | 0.449 |
MOD_GlcNHglycan | 196 | 199 | PF01048 | 0.713 |
MOD_GlcNHglycan | 214 | 217 | PF01048 | 0.715 |
MOD_GlcNHglycan | 228 | 231 | PF01048 | 0.582 |
MOD_GlcNHglycan | 261 | 264 | PF01048 | 0.370 |
MOD_GlcNHglycan | 299 | 302 | PF01048 | 0.267 |
MOD_GlcNHglycan | 325 | 328 | PF01048 | 0.301 |
MOD_GlcNHglycan | 336 | 340 | PF01048 | 0.293 |
MOD_GlcNHglycan | 483 | 486 | PF01048 | 0.380 |
MOD_GlcNHglycan | 546 | 549 | PF01048 | 0.756 |
MOD_GlcNHglycan | 557 | 560 | PF01048 | 0.666 |
MOD_GlcNHglycan | 563 | 566 | PF01048 | 0.593 |
MOD_GlcNHglycan | 582 | 585 | PF01048 | 0.314 |
MOD_GlcNHglycan | 603 | 606 | PF01048 | 0.610 |
MOD_GlcNHglycan | 630 | 633 | PF01048 | 0.499 |
MOD_GlcNHglycan | 682 | 686 | PF01048 | 0.518 |
MOD_GSK3_1 | 110 | 117 | PF00069 | 0.620 |
MOD_GSK3_1 | 127 | 134 | PF00069 | 0.451 |
MOD_GSK3_1 | 212 | 219 | PF00069 | 0.576 |
MOD_GSK3_1 | 220 | 227 | PF00069 | 0.590 |
MOD_GSK3_1 | 488 | 495 | PF00069 | 0.375 |
MOD_GSK3_1 | 525 | 532 | PF00069 | 0.394 |
MOD_GSK3_1 | 555 | 562 | PF00069 | 0.728 |
MOD_GSK3_1 | 597 | 604 | PF00069 | 0.539 |
MOD_GSK3_1 | 689 | 696 | PF00069 | 0.388 |
MOD_GSK3_1 | 699 | 706 | PF00069 | 0.330 |
MOD_N-GLC_1 | 182 | 187 | PF02516 | 0.641 |
MOD_N-GLC_1 | 32 | 37 | PF02516 | 0.569 |
MOD_N-GLC_1 | 488 | 493 | PF02516 | 0.286 |
MOD_NEK2_1 | 110 | 115 | PF00069 | 0.577 |
MOD_NEK2_1 | 297 | 302 | PF00069 | 0.386 |
MOD_NEK2_1 | 323 | 328 | PF00069 | 0.314 |
MOD_NEK2_1 | 469 | 474 | PF00069 | 0.245 |
MOD_NEK2_1 | 525 | 530 | PF00069 | 0.295 |
MOD_NEK2_1 | 627 | 632 | PF00069 | 0.415 |
MOD_NEK2_2 | 169 | 174 | PF00069 | 0.486 |
MOD_NEK2_2 | 191 | 196 | PF00069 | 0.460 |
MOD_NEK2_2 | 431 | 436 | PF00069 | 0.377 |
MOD_NEK2_2 | 517 | 522 | PF00069 | 0.383 |
MOD_NEK2_2 | 703 | 708 | PF00069 | 0.412 |
MOD_PK_1 | 273 | 279 | PF00069 | 0.249 |
MOD_PKA_2 | 169 | 175 | PF00069 | 0.389 |
MOD_PKA_2 | 204 | 210 | PF00069 | 0.659 |
MOD_PKA_2 | 278 | 284 | PF00069 | 0.260 |
MOD_PKA_2 | 323 | 329 | PF00069 | 0.432 |
MOD_PKA_2 | 406 | 412 | PF00069 | 0.311 |
MOD_PKA_2 | 469 | 475 | PF00069 | 0.345 |
MOD_PKA_2 | 61 | 67 | PF00069 | 0.540 |
MOD_PKA_2 | 627 | 633 | PF00069 | 0.467 |
MOD_PKA_2 | 654 | 660 | PF00069 | 0.452 |
MOD_PKA_2 | 689 | 695 | PF00069 | 0.442 |
MOD_PKB_1 | 672 | 680 | PF00069 | 0.406 |
MOD_Plk_1 | 182 | 188 | PF00069 | 0.592 |
MOD_Plk_1 | 32 | 38 | PF00069 | 0.567 |
MOD_Plk_1 | 598 | 604 | PF00069 | 0.479 |
MOD_Plk_1 | 657 | 663 | PF00069 | 0.571 |
MOD_Plk_4 | 32 | 38 | PF00069 | 0.621 |
MOD_Plk_4 | 517 | 523 | PF00069 | 0.301 |
MOD_Plk_4 | 525 | 531 | PF00069 | 0.306 |
MOD_Plk_4 | 606 | 612 | PF00069 | 0.277 |
MOD_Plk_4 | 657 | 663 | PF00069 | 0.352 |
MOD_Plk_4 | 703 | 709 | PF00069 | 0.338 |
MOD_ProDKin_1 | 18 | 24 | PF00069 | 0.577 |
MOD_ProDKin_1 | 216 | 222 | PF00069 | 0.718 |
MOD_ProDKin_1 | 26 | 32 | PF00069 | 0.513 |
MOD_ProDKin_1 | 359 | 365 | PF00069 | 0.324 |
TRG_DiLeu_BaEn_1 | 248 | 253 | PF01217 | 0.260 |
TRG_DiLeu_BaEn_2 | 381 | 387 | PF01217 | 0.264 |
TRG_DiLeu_BaEn_4 | 378 | 384 | PF01217 | 0.217 |
TRG_ENDOCYTIC_2 | 159 | 162 | PF00928 | 0.368 |
TRG_ENDOCYTIC_2 | 234 | 237 | PF00928 | 0.332 |
TRG_ENDOCYTIC_2 | 256 | 259 | PF00928 | 0.320 |
TRG_ENDOCYTIC_2 | 319 | 322 | PF00928 | 0.264 |
TRG_ENDOCYTIC_2 | 443 | 446 | PF00928 | 0.260 |
TRG_ENDOCYTIC_2 | 45 | 48 | PF00928 | 0.349 |
TRG_ENDOCYTIC_2 | 704 | 707 | PF00928 | 0.341 |
TRG_ER_diArg_1 | 122 | 124 | PF00400 | 0.637 |
TRG_ER_diArg_1 | 147 | 149 | PF00400 | 0.427 |
TRG_ER_diArg_1 | 155 | 157 | PF00400 | 0.400 |
TRG_ER_diArg_1 | 175 | 178 | PF00400 | 0.366 |
TRG_ER_diArg_1 | 205 | 208 | PF00400 | 0.607 |
TRG_ER_diArg_1 | 239 | 242 | PF00400 | 0.285 |
TRG_ER_diArg_1 | 344 | 347 | PF00400 | 0.324 |
TRG_ER_diArg_1 | 357 | 359 | PF00400 | 0.348 |
TRG_ER_diArg_1 | 389 | 391 | PF00400 | 0.313 |
TRG_ER_diArg_1 | 638 | 640 | PF00400 | 0.558 |
TRG_ER_diArg_1 | 672 | 674 | PF00400 | 0.474 |
TRG_NES_CRM1_1 | 248 | 261 | PF08389 | 0.285 |
TRG_NLS_MonoExtC_3 | 239 | 245 | PF00514 | 0.260 |
TRG_Pf-PMV_PEXEL_1 | 250 | 255 | PF00026 | 0.260 |
TRG_Pf-PMV_PEXEL_1 | 74 | 78 | PF00026 | 0.571 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4F4 | Leptomonas seymouri | 49% | 75% |
A0A1X0NRV3 | Trypanosomatidae | 33% | 100% |
A0A3R7LD82 | Trypanosoma rangeli | 33% | 100% |
A0A3S7X658 | Leishmania donovani | 88% | 100% |
A4HKY3 | Leishmania braziliensis | 73% | 100% |
A4I8G2 | Leishmania infantum | 88% | 77% |
D0AAQ9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
Q08647 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 21% | 100% |
Q4Q4T4 | Leishmania major | 86% | 98% |