RNA Processing, Pseudouridine synthase Uncharacterized
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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: A4I245
Term | Name | Level | Count |
---|---|---|---|
GO:0001522 | pseudouridine synthesis | 6 | 7 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 7 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 7 |
GO:0006807 | nitrogen compound metabolic process | 2 | 7 |
GO:0008152 | metabolic process | 1 | 7 |
GO:0009451 | RNA modification | 5 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0016070 | RNA metabolic process | 5 | 7 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 7 |
GO:0043170 | macromolecule metabolic process | 3 | 7 |
GO:0043412 | macromolecule modification | 4 | 7 |
GO:0044237 | cellular metabolic process | 2 | 7 |
GO:0044238 | primary metabolic process | 2 | 7 |
GO:0046483 | heterocycle metabolic process | 3 | 7 |
GO:0071704 | organic substance metabolic process | 2 | 7 |
GO:0090304 | nucleic acid metabolic process | 4 | 7 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 7 |
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 | 7 |
GO:0003723 | RNA binding | 4 | 7 |
GO:0003824 | catalytic activity | 1 | 7 |
GO:0005488 | binding | 1 | 7 |
GO:0009982 | pseudouridine synthase activity | 4 | 7 |
GO:0016853 | isomerase activity | 2 | 7 |
GO:0016866 | intramolecular transferase activity | 3 | 7 |
GO:0097159 | organic cyclic compound binding | 2 | 7 |
GO:1901363 | heterocyclic compound binding | 2 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 222 | 226 | PF00656 | 0.702 |
CLV_NRD_NRD_1 | 171 | 173 | PF00675 | 0.308 |
CLV_NRD_NRD_1 | 178 | 180 | PF00675 | 0.424 |
CLV_NRD_NRD_1 | 195 | 197 | PF00675 | 0.459 |
CLV_NRD_NRD_1 | 554 | 556 | PF00675 | 0.767 |
CLV_NRD_NRD_1 | 736 | 738 | PF00675 | 0.425 |
CLV_PCSK_KEX2_1 | 171 | 173 | PF00082 | 0.292 |
CLV_PCSK_KEX2_1 | 194 | 196 | PF00082 | 0.614 |
CLV_PCSK_KEX2_1 | 52 | 54 | PF00082 | 0.292 |
CLV_PCSK_KEX2_1 | 554 | 556 | PF00082 | 0.703 |
CLV_PCSK_KEX2_1 | 576 | 578 | PF00082 | 0.618 |
CLV_PCSK_KEX2_1 | 736 | 738 | PF00082 | 0.425 |
CLV_PCSK_PC1ET2_1 | 52 | 54 | PF00082 | 0.376 |
CLV_PCSK_PC1ET2_1 | 576 | 578 | PF00082 | 0.618 |
CLV_PCSK_SKI1_1 | 179 | 183 | PF00082 | 0.545 |
CLV_PCSK_SKI1_1 | 559 | 563 | PF00082 | 0.693 |
CLV_PCSK_SKI1_1 | 573 | 577 | PF00082 | 0.526 |
CLV_PCSK_SKI1_1 | 671 | 675 | PF00082 | 0.543 |
CLV_Separin_Metazoa | 191 | 195 | PF03568 | 0.588 |
DEG_APCC_DBOX_1 | 432 | 440 | PF00400 | 0.453 |
DEG_Nend_UBRbox_4 | 1 | 3 | PF02207 | 0.472 |
DEG_ODPH_VHL_1 | 49 | 60 | PF01847 | 0.576 |
DEG_SCF_FBW7_2 | 211 | 216 | PF00400 | 0.761 |
DEG_SPOP_SBC_1 | 459 | 463 | PF00917 | 0.605 |
DEG_SPOP_SBC_1 | 711 | 715 | PF00917 | 0.578 |
DOC_ANK_TNKS_1 | 736 | 743 | PF00023 | 0.424 |
DOC_CDC14_PxL_1 | 389 | 397 | PF14671 | 0.534 |
DOC_CKS1_1 | 287 | 292 | PF01111 | 0.713 |
DOC_CKS1_1 | 421 | 426 | PF01111 | 0.439 |
DOC_CYCLIN_yCln2_LP_2 | 304 | 310 | PF00134 | 0.701 |
DOC_MAPK_gen_1 | 152 | 162 | PF00069 | 0.492 |
DOC_MAPK_gen_1 | 510 | 518 | PF00069 | 0.556 |
DOC_MAPK_gen_1 | 52 | 60 | PF00069 | 0.576 |
DOC_PP2B_LxvP_1 | 302 | 305 | PF13499 | 0.675 |
DOC_PP4_FxxP_1 | 390 | 393 | PF00568 | 0.614 |
DOC_PP4_FxxP_1 | 747 | 750 | PF00568 | 0.428 |
DOC_USP7_MATH_1 | 125 | 129 | PF00917 | 0.485 |
DOC_USP7_MATH_1 | 199 | 203 | PF00917 | 0.697 |
DOC_USP7_MATH_1 | 221 | 225 | PF00917 | 0.626 |
DOC_USP7_MATH_1 | 325 | 329 | PF00917 | 0.524 |
DOC_USP7_MATH_1 | 374 | 378 | PF00917 | 0.628 |
DOC_USP7_MATH_1 | 407 | 411 | PF00917 | 0.648 |
DOC_USP7_MATH_1 | 450 | 454 | PF00917 | 0.522 |
DOC_USP7_MATH_1 | 459 | 463 | PF00917 | 0.651 |
DOC_USP7_MATH_1 | 550 | 554 | PF00917 | 0.793 |
DOC_USP7_MATH_1 | 580 | 584 | PF00917 | 0.633 |
DOC_USP7_MATH_1 | 605 | 609 | PF00917 | 0.665 |
DOC_USP7_MATH_1 | 623 | 627 | PF00917 | 0.547 |
DOC_USP7_MATH_1 | 700 | 704 | PF00917 | 0.696 |
DOC_USP7_MATH_1 | 709 | 713 | PF00917 | 0.654 |
DOC_WW_Pin1_4 | 209 | 214 | PF00397 | 0.759 |
DOC_WW_Pin1_4 | 217 | 222 | PF00397 | 0.660 |
DOC_WW_Pin1_4 | 236 | 241 | PF00397 | 0.648 |
DOC_WW_Pin1_4 | 286 | 291 | PF00397 | 0.753 |
DOC_WW_Pin1_4 | 294 | 299 | PF00397 | 0.698 |
DOC_WW_Pin1_4 | 375 | 380 | PF00397 | 0.655 |
DOC_WW_Pin1_4 | 420 | 425 | PF00397 | 0.439 |
DOC_WW_Pin1_4 | 485 | 490 | PF00397 | 0.625 |
DOC_WW_Pin1_4 | 548 | 553 | PF00397 | 0.748 |
DOC_WW_Pin1_4 | 685 | 690 | PF00397 | 0.696 |
DOC_WW_Pin1_4 | 702 | 707 | PF00397 | 0.505 |
DOC_WW_Pin1_4 | 72 | 77 | PF00397 | 0.545 |
LIG_14-3-3_CanoR_1 | 249 | 257 | PF00244 | 0.459 |
LIG_14-3-3_CanoR_1 | 329 | 337 | PF00244 | 0.556 |
LIG_14-3-3_CanoR_1 | 433 | 443 | PF00244 | 0.437 |
LIG_14-3-3_CanoR_1 | 529 | 535 | PF00244 | 0.523 |
LIG_14-3-3_CanoR_1 | 559 | 564 | PF00244 | 0.692 |
LIG_14-3-3_CanoR_1 | 94 | 100 | PF00244 | 0.515 |
LIG_APCC_ABBAyCdc20_2 | 513 | 519 | PF00400 | 0.573 |
LIG_BIR_III_4 | 564 | 568 | PF00653 | 0.668 |
LIG_FHA_1 | 155 | 161 | PF00498 | 0.492 |
LIG_FHA_1 | 187 | 193 | PF00498 | 0.496 |
LIG_FHA_1 | 252 | 258 | PF00498 | 0.438 |
LIG_FHA_1 | 364 | 370 | PF00498 | 0.558 |
LIG_FHA_1 | 40 | 46 | PF00498 | 0.492 |
LIG_FHA_1 | 424 | 430 | PF00498 | 0.530 |
LIG_FHA_1 | 570 | 576 | PF00498 | 0.555 |
LIG_FHA_1 | 607 | 613 | PF00498 | 0.671 |
LIG_FHA_1 | 656 | 662 | PF00498 | 0.593 |
LIG_FHA_1 | 69 | 75 | PF00498 | 0.492 |
LIG_LIR_Gen_1 | 514 | 523 | PF02991 | 0.567 |
LIG_LIR_Nem_3 | 514 | 518 | PF02991 | 0.578 |
LIG_LIR_Nem_3 | 81 | 86 | PF02991 | 0.491 |
LIG_NRBOX | 384 | 390 | PF00104 | 0.636 |
LIG_NRBOX | 40 | 46 | PF00104 | 0.576 |
LIG_NRP_CendR_1 | 756 | 757 | PF00754 | 0.627 |
LIG_PTAP_UEV_1 | 88 | 93 | PF05743 | 0.451 |
LIG_SH2_CRK | 17 | 21 | PF00017 | 0.335 |
LIG_SH2_CRK | 38 | 42 | PF00017 | 0.492 |
LIG_SH2_CRK | 86 | 90 | PF00017 | 0.476 |
LIG_SH2_GRB2like | 37 | 40 | PF00017 | 0.576 |
LIG_SH2_NCK_1 | 640 | 644 | PF00017 | 0.569 |
LIG_SH2_NCK_1 | 86 | 90 | PF00017 | 0.530 |
LIG_SH2_SRC | 86 | 89 | PF00017 | 0.576 |
LIG_SH2_STAP1 | 83 | 87 | PF00017 | 0.576 |
LIG_SH2_STAT3 | 255 | 258 | PF00017 | 0.426 |
LIG_SH2_STAT5 | 123 | 126 | PF00017 | 0.530 |
LIG_SH2_STAT5 | 261 | 264 | PF00017 | 0.429 |
LIG_SH2_STAT5 | 326 | 329 | PF00017 | 0.603 |
LIG_SH2_STAT5 | 425 | 428 | PF00017 | 0.475 |
LIG_SH2_STAT5 | 47 | 50 | PF00017 | 0.541 |
LIG_SH2_STAT5 | 530 | 533 | PF00017 | 0.644 |
LIG_SH3_1 | 86 | 92 | PF00018 | 0.530 |
LIG_SH3_2 | 89 | 94 | PF14604 | 0.530 |
LIG_SH3_3 | 143 | 149 | PF00018 | 0.576 |
LIG_SH3_3 | 19 | 25 | PF00018 | 0.576 |
LIG_SH3_3 | 230 | 236 | PF00018 | 0.729 |
LIG_SH3_3 | 237 | 243 | PF00018 | 0.581 |
LIG_SH3_3 | 287 | 293 | PF00018 | 0.777 |
LIG_SH3_3 | 295 | 301 | PF00018 | 0.762 |
LIG_SH3_3 | 364 | 370 | PF00018 | 0.678 |
LIG_SH3_3 | 45 | 51 | PF00018 | 0.492 |
LIG_SH3_3 | 465 | 471 | PF00018 | 0.632 |
LIG_SH3_3 | 57 | 63 | PF00018 | 0.492 |
LIG_SH3_3 | 613 | 619 | PF00018 | 0.569 |
LIG_SH3_3 | 703 | 709 | PF00018 | 0.647 |
LIG_SH3_3 | 86 | 92 | PF00018 | 0.553 |
LIG_SH3_3 | 96 | 102 | PF00018 | 0.502 |
LIG_Sin3_3 | 4 | 11 | PF02671 | 0.447 |
LIG_SUMO_SIM_anti_2 | 157 | 164 | PF11976 | 0.492 |
LIG_TRAF2_1 | 414 | 417 | PF00917 | 0.526 |
LIG_TRAF2_1 | 537 | 540 | PF00917 | 0.485 |
LIG_TRFH_1 | 47 | 51 | PF08558 | 0.492 |
LIG_WW_3 | 94 | 98 | PF00397 | 0.451 |
MOD_CDC14_SPxK_1 | 488 | 491 | PF00782 | 0.598 |
MOD_CDC14_SPxK_1 | 551 | 554 | PF00782 | 0.699 |
MOD_CDK_SPK_2 | 689 | 694 | PF00069 | 0.573 |
MOD_CDK_SPxK_1 | 485 | 491 | PF00069 | 0.600 |
MOD_CDK_SPxK_1 | 548 | 554 | PF00069 | 0.687 |
MOD_CDK_SPxxK_3 | 548 | 555 | PF00069 | 0.754 |
MOD_CDK_SPxxK_3 | 72 | 79 | PF00069 | 0.530 |
MOD_CK1_1 | 116 | 122 | PF00069 | 0.520 |
MOD_CK1_1 | 128 | 134 | PF00069 | 0.437 |
MOD_CK1_1 | 276 | 282 | PF00069 | 0.756 |
MOD_CK1_1 | 40 | 46 | PF00069 | 0.530 |
MOD_CK1_1 | 410 | 416 | PF00069 | 0.529 |
MOD_CK1_1 | 67 | 73 | PF00069 | 0.484 |
MOD_CK1_1 | 684 | 690 | PF00069 | 0.730 |
MOD_CK1_1 | 712 | 718 | PF00069 | 0.578 |
MOD_CK2_1 | 128 | 134 | PF00069 | 0.455 |
MOD_CK2_1 | 250 | 256 | PF00069 | 0.600 |
MOD_CK2_1 | 40 | 46 | PF00069 | 0.530 |
MOD_CK2_1 | 410 | 416 | PF00069 | 0.636 |
MOD_CK2_1 | 710 | 716 | PF00069 | 0.660 |
MOD_CK2_1 | 72 | 78 | PF00069 | 0.492 |
MOD_GlcNHglycan | 116 | 119 | PF01048 | 0.321 |
MOD_GlcNHglycan | 129 | 133 | PF01048 | 0.249 |
MOD_GlcNHglycan | 157 | 160 | PF01048 | 0.292 |
MOD_GlcNHglycan | 268 | 271 | PF01048 | 0.592 |
MOD_GlcNHglycan | 275 | 278 | PF01048 | 0.644 |
MOD_GlcNHglycan | 332 | 335 | PF01048 | 0.569 |
MOD_GlcNHglycan | 352 | 355 | PF01048 | 0.713 |
MOD_GlcNHglycan | 396 | 399 | PF01048 | 0.699 |
MOD_GlcNHglycan | 412 | 415 | PF01048 | 0.549 |
MOD_GlcNHglycan | 452 | 455 | PF01048 | 0.714 |
MOD_GlcNHglycan | 479 | 482 | PF01048 | 0.616 |
MOD_GlcNHglycan | 499 | 503 | PF01048 | 0.585 |
MOD_GlcNHglycan | 658 | 661 | PF01048 | 0.460 |
MOD_GlcNHglycan | 719 | 722 | PF01048 | 0.702 |
MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.237 |
MOD_GSK3_1 | 110 | 117 | PF00069 | 0.562 |
MOD_GSK3_1 | 124 | 131 | PF00069 | 0.427 |
MOD_GSK3_1 | 217 | 224 | PF00069 | 0.701 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.492 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.656 |
MOD_GSK3_1 | 325 | 332 | PF00069 | 0.543 |
MOD_GSK3_1 | 406 | 413 | PF00069 | 0.736 |
MOD_GSK3_1 | 475 | 482 | PF00069 | 0.762 |
MOD_GSK3_1 | 64 | 71 | PF00069 | 0.490 |
MOD_GSK3_1 | 681 | 688 | PF00069 | 0.735 |
MOD_GSK3_1 | 698 | 705 | PF00069 | 0.528 |
MOD_N-GLC_1 | 199 | 204 | PF02516 | 0.571 |
MOD_N-GLC_1 | 725 | 730 | PF02516 | 0.665 |
MOD_NEK2_1 | 330 | 335 | PF00069 | 0.550 |
MOD_NEK2_1 | 434 | 439 | PF00069 | 0.581 |
MOD_NEK2_1 | 606 | 611 | PF00069 | 0.671 |
MOD_NEK2_1 | 64 | 69 | PF00069 | 0.484 |
MOD_NEK2_1 | 698 | 703 | PF00069 | 0.662 |
MOD_NEK2_2 | 530 | 535 | PF00069 | 0.576 |
MOD_PIKK_1 | 461 | 467 | PF00454 | 0.669 |
MOD_PK_1 | 172 | 178 | PF00069 | 0.530 |
MOD_PKA_2 | 506 | 512 | PF00069 | 0.696 |
MOD_PKB_1 | 264 | 272 | PF00069 | 0.657 |
MOD_Plk_4 | 172 | 178 | PF00069 | 0.481 |
MOD_Plk_4 | 40 | 46 | PF00069 | 0.530 |
MOD_Plk_4 | 64 | 70 | PF00069 | 0.484 |
MOD_ProDKin_1 | 209 | 215 | PF00069 | 0.756 |
MOD_ProDKin_1 | 217 | 223 | PF00069 | 0.660 |
MOD_ProDKin_1 | 236 | 242 | PF00069 | 0.640 |
MOD_ProDKin_1 | 286 | 292 | PF00069 | 0.753 |
MOD_ProDKin_1 | 294 | 300 | PF00069 | 0.698 |
MOD_ProDKin_1 | 375 | 381 | PF00069 | 0.649 |
MOD_ProDKin_1 | 420 | 426 | PF00069 | 0.440 |
MOD_ProDKin_1 | 485 | 491 | PF00069 | 0.625 |
MOD_ProDKin_1 | 548 | 554 | PF00069 | 0.751 |
MOD_ProDKin_1 | 685 | 691 | PF00069 | 0.694 |
MOD_ProDKin_1 | 702 | 708 | PF00069 | 0.508 |
MOD_ProDKin_1 | 72 | 78 | PF00069 | 0.545 |
MOD_SUMO_rev_2 | 594 | 604 | PF00179 | 0.598 |
TRG_DiLeu_BaEn_4 | 416 | 422 | PF01217 | 0.577 |
TRG_DiLeu_BaLyEn_6 | 60 | 65 | PF01217 | 0.492 |
TRG_ENDOCYTIC_2 | 17 | 20 | PF00928 | 0.355 |
TRG_ENDOCYTIC_2 | 38 | 41 | PF00928 | 0.492 |
TRG_ER_diArg_1 | 171 | 173 | PF00400 | 0.508 |
TRG_ER_diArg_1 | 193 | 196 | PF00400 | 0.607 |
TRG_ER_diArg_1 | 264 | 267 | PF00400 | 0.591 |
TRG_ER_diArg_1 | 343 | 346 | PF00400 | 0.622 |
TRG_ER_diArg_1 | 471 | 474 | PF00400 | 0.598 |
TRG_ER_diArg_1 | 736 | 738 | PF00400 | 0.495 |
TRG_ER_diArg_1 | 755 | 757 | PF00400 | 0.575 |
TRG_NLS_MonoExtN_4 | 573 | 580 | PF00514 | 0.674 |
TRG_Pf-PMV_PEXEL_1 | 736 | 741 | PF00026 | 0.449 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IHN9 | Leptomonas seymouri | 39% | 94% |
A0A3Q8IC63 | Leishmania donovani | 100% | 78% |
A4HEX1 | Leishmania braziliensis | 68% | 100% |
E9AY95 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
Q4Q978 | Leishmania major | 87% | 100% |