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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005829 | cytosol | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4QG75
Term | Name | Level | Count |
---|---|---|---|
GO:0002097 | tRNA wobble base modification | 7 | 7 |
GO:0002098 | tRNA wobble uridine modification | 8 | 7 |
GO:0002143 | tRNA wobble position uridine thiolation | 8 | 2 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 7 |
GO:0006396 | RNA processing | 6 | 7 |
GO:0006399 | tRNA metabolic process | 7 | 7 |
GO:0006400 | tRNA modification | 6 | 7 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 7 |
GO:0006807 | nitrogen compound metabolic process | 2 | 7 |
GO:0008033 | tRNA processing | 8 | 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:0034227 | tRNA thio-modification | 7 | 7 |
GO:0034470 | ncRNA processing | 7 | 7 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 7 |
GO:0034660 | ncRNA metabolic process | 6 | 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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000049 | tRNA binding | 5 | 7 |
GO:0003676 | nucleic acid binding | 3 | 7 |
GO:0003723 | RNA binding | 4 | 7 |
GO:0003824 | catalytic activity | 1 | 2 |
GO:0005488 | binding | 1 | 7 |
GO:0016740 | transferase activity | 2 | 2 |
GO:0016782 | transferase activity, transferring sulphur-containing groups | 3 | 2 |
GO:0016783 | sulfurtransferase activity | 4 | 2 |
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 | 615 | 619 | PF00656 | 0.630 |
CLV_NRD_NRD_1 | 172 | 174 | PF00675 | 0.557 |
CLV_NRD_NRD_1 | 523 | 525 | PF00675 | 0.637 |
CLV_NRD_NRD_1 | 548 | 550 | PF00675 | 0.553 |
CLV_NRD_NRD_1 | 82 | 84 | PF00675 | 0.557 |
CLV_PCSK_KEX2_1 | 194 | 196 | PF00082 | 0.612 |
CLV_PCSK_KEX2_1 | 548 | 550 | PF00082 | 0.553 |
CLV_PCSK_KEX2_1 | 82 | 84 | PF00082 | 0.557 |
CLV_PCSK_PC1ET2_1 | 194 | 196 | PF00082 | 0.609 |
CLV_PCSK_PC7_1 | 78 | 84 | PF00082 | 0.492 |
CLV_PCSK_SKI1_1 | 282 | 286 | PF00082 | 0.527 |
CLV_PCSK_SKI1_1 | 295 | 299 | PF00082 | 0.376 |
CLV_PCSK_SKI1_1 | 381 | 385 | PF00082 | 0.300 |
CLV_PCSK_SKI1_1 | 406 | 410 | PF00082 | 0.390 |
CLV_PCSK_SKI1_1 | 419 | 423 | PF00082 | 0.475 |
CLV_PCSK_SKI1_1 | 524 | 528 | PF00082 | 0.693 |
CLV_Separin_Metazoa | 490 | 494 | PF03568 | 0.544 |
DEG_APCC_DBOX_1 | 547 | 555 | PF00400 | 0.518 |
DEG_SCF_FBW7_1 | 219 | 225 | PF00400 | 0.711 |
DEG_SCF_FBW7_1 | 604 | 609 | PF00400 | 0.644 |
DEG_SPOP_SBC_1 | 137 | 141 | PF00917 | 0.676 |
DOC_CKS1_1 | 219 | 224 | PF01111 | 0.709 |
DOC_CYCLIN_yCln2_LP_2 | 130 | 136 | PF00134 | 0.436 |
DOC_CYCLIN_yCln2_LP_2 | 541 | 547 | PF00134 | 0.654 |
DOC_MAPK_gen_1 | 368 | 375 | PF00069 | 0.440 |
DOC_MAPK_gen_1 | 548 | 556 | PF00069 | 0.517 |
DOC_PP2B_LxvP_1 | 130 | 133 | PF13499 | 0.458 |
DOC_PP2B_LxvP_1 | 134 | 137 | PF13499 | 0.576 |
DOC_PP2B_LxvP_1 | 541 | 544 | PF13499 | 0.653 |
DOC_USP7_MATH_1 | 108 | 112 | PF00917 | 0.630 |
DOC_USP7_MATH_1 | 113 | 117 | PF00917 | 0.549 |
DOC_USP7_MATH_1 | 137 | 141 | PF00917 | 0.619 |
DOC_USP7_MATH_1 | 245 | 249 | PF00917 | 0.761 |
DOC_USP7_MATH_1 | 347 | 351 | PF00917 | 0.720 |
DOC_USP7_MATH_1 | 448 | 452 | PF00917 | 0.538 |
DOC_USP7_MATH_1 | 606 | 610 | PF00917 | 0.691 |
DOC_USP7_MATH_1 | 611 | 615 | PF00917 | 0.642 |
DOC_USP7_MATH_1 | 620 | 624 | PF00917 | 0.667 |
DOC_USP7_MATH_1 | 678 | 682 | PF00917 | 0.581 |
DOC_USP7_UBL2_3 | 194 | 198 | PF12436 | 0.716 |
DOC_USP7_UBL2_3 | 521 | 525 | PF12436 | 0.696 |
DOC_WW_Pin1_4 | 109 | 114 | PF00397 | 0.571 |
DOC_WW_Pin1_4 | 141 | 146 | PF00397 | 0.657 |
DOC_WW_Pin1_4 | 218 | 223 | PF00397 | 0.708 |
DOC_WW_Pin1_4 | 233 | 238 | PF00397 | 0.541 |
DOC_WW_Pin1_4 | 437 | 442 | PF00397 | 0.460 |
DOC_WW_Pin1_4 | 48 | 53 | PF00397 | 0.427 |
DOC_WW_Pin1_4 | 602 | 607 | PF00397 | 0.683 |
DOC_WW_Pin1_4 | 609 | 614 | PF00397 | 0.622 |
DOC_WW_Pin1_4 | 623 | 628 | PF00397 | 0.477 |
DOC_WW_Pin1_4 | 84 | 89 | PF00397 | 0.570 |
DOC_WW_Pin1_4 | 99 | 104 | PF00397 | 0.565 |
LIG_14-3-3_CanoR_1 | 160 | 169 | PF00244 | 0.492 |
LIG_14-3-3_CanoR_1 | 289 | 299 | PF00244 | 0.412 |
LIG_14-3-3_CanoR_1 | 303 | 308 | PF00244 | 0.416 |
LIG_14-3-3_CanoR_1 | 381 | 390 | PF00244 | 0.312 |
LIG_14-3-3_CanoR_1 | 406 | 415 | PF00244 | 0.479 |
LIG_BIR_III_2 | 643 | 647 | PF00653 | 0.495 |
LIG_CSL_BTD_1 | 644 | 647 | PF09270 | 0.495 |
LIG_deltaCOP1_diTrp_1 | 643 | 650 | PF00928 | 0.560 |
LIG_EVH1_1 | 132 | 136 | PF00568 | 0.592 |
LIG_EVH1_2 | 646 | 650 | PF00568 | 0.532 |
LIG_FHA_1 | 219 | 225 | PF00498 | 0.628 |
LIG_FHA_1 | 253 | 259 | PF00498 | 0.566 |
LIG_FHA_1 | 327 | 333 | PF00498 | 0.414 |
LIG_FHA_1 | 382 | 388 | PF00498 | 0.301 |
LIG_FHA_1 | 407 | 413 | PF00498 | 0.487 |
LIG_FHA_1 | 438 | 444 | PF00498 | 0.474 |
LIG_FHA_1 | 447 | 453 | PF00498 | 0.459 |
LIG_FHA_1 | 529 | 535 | PF00498 | 0.527 |
LIG_FHA_1 | 680 | 686 | PF00498 | 0.552 |
LIG_FHA_2 | 202 | 208 | PF00498 | 0.574 |
LIG_FHA_2 | 613 | 619 | PF00498 | 0.624 |
LIG_FHA_2 | 654 | 660 | PF00498 | 0.660 |
LIG_LIR_Gen_1 | 166 | 176 | PF02991 | 0.488 |
LIG_LIR_Gen_1 | 296 | 307 | PF02991 | 0.486 |
LIG_LIR_Gen_1 | 426 | 436 | PF02991 | 0.392 |
LIG_LIR_Gen_1 | 469 | 478 | PF02991 | 0.379 |
LIG_LIR_Nem_3 | 166 | 172 | PF02991 | 0.488 |
LIG_LIR_Nem_3 | 27 | 32 | PF02991 | 0.368 |
LIG_LIR_Nem_3 | 296 | 302 | PF02991 | 0.414 |
LIG_LIR_Nem_3 | 426 | 432 | PF02991 | 0.389 |
LIG_LIR_Nem_3 | 469 | 475 | PF02991 | 0.371 |
LIG_LIR_Nem_3 | 630 | 636 | PF02991 | 0.416 |
LIG_SH2_CRK | 299 | 303 | PF00017 | 0.410 |
LIG_SH2_CRK | 429 | 433 | PF00017 | 0.460 |
LIG_SH2_STAP1 | 269 | 273 | PF00017 | 0.466 |
LIG_SH2_STAP1 | 283 | 287 | PF00017 | 0.369 |
LIG_SH2_STAT3 | 175 | 178 | PF00017 | 0.512 |
LIG_SH2_STAT3 | 581 | 584 | PF00017 | 0.483 |
LIG_SH2_STAT3 | 636 | 639 | PF00017 | 0.448 |
LIG_SH2_STAT5 | 175 | 178 | PF00017 | 0.560 |
LIG_SH2_STAT5 | 24 | 27 | PF00017 | 0.360 |
LIG_SH2_STAT5 | 277 | 280 | PF00017 | 0.404 |
LIG_SH2_STAT5 | 32 | 35 | PF00017 | 0.354 |
LIG_SH2_STAT5 | 429 | 432 | PF00017 | 0.448 |
LIG_SH2_STAT5 | 439 | 442 | PF00017 | 0.421 |
LIG_SH3_3 | 130 | 136 | PF00018 | 0.494 |
LIG_SH3_CIN85_PxpxPR_1 | 235 | 240 | PF14604 | 0.591 |
LIG_SUMO_SIM_anti_2 | 116 | 122 | PF11976 | 0.482 |
LIG_SUMO_SIM_par_1 | 594 | 602 | PF11976 | 0.598 |
LIG_TRAF2_1 | 164 | 167 | PF00917 | 0.483 |
LIG_TRAF2_1 | 337 | 340 | PF00917 | 0.706 |
LIG_TRAF2_1 | 487 | 490 | PF00917 | 0.505 |
LIG_TYR_ITIM | 427 | 432 | PF00017 | 0.468 |
LIG_WW_3 | 179 | 183 | PF00397 | 0.587 |
MOD_CDK_SPK_2 | 602 | 607 | PF00069 | 0.683 |
MOD_CDK_SPxK_1 | 84 | 90 | PF00069 | 0.578 |
MOD_CDK_SPxxK_3 | 103 | 110 | PF00069 | 0.653 |
MOD_CDK_SPxxK_3 | 233 | 240 | PF00069 | 0.591 |
MOD_CK1_1 | 139 | 145 | PF00069 | 0.674 |
MOD_CK1_1 | 233 | 239 | PF00069 | 0.696 |
MOD_CK1_1 | 248 | 254 | PF00069 | 0.532 |
MOD_CK1_1 | 288 | 294 | PF00069 | 0.437 |
MOD_CK1_1 | 466 | 472 | PF00069 | 0.562 |
MOD_CK1_1 | 515 | 521 | PF00069 | 0.604 |
MOD_CK1_1 | 576 | 582 | PF00069 | 0.513 |
MOD_CK1_1 | 602 | 608 | PF00069 | 0.670 |
MOD_CK1_1 | 609 | 615 | PF00069 | 0.607 |
MOD_CK1_1 | 623 | 629 | PF00069 | 0.488 |
MOD_CK1_1 | 99 | 105 | PF00069 | 0.715 |
MOD_CK2_1 | 160 | 166 | PF00069 | 0.485 |
MOD_CK2_1 | 201 | 207 | PF00069 | 0.574 |
MOD_CK2_1 | 290 | 296 | PF00069 | 0.423 |
MOD_CK2_1 | 618 | 624 | PF00069 | 0.617 |
MOD_CK2_1 | 651 | 657 | PF00069 | 0.793 |
MOD_GlcNHglycan | 151 | 154 | PF01048 | 0.617 |
MOD_GlcNHglycan | 162 | 165 | PF01048 | 0.444 |
MOD_GlcNHglycan | 232 | 235 | PF01048 | 0.696 |
MOD_GlcNHglycan | 247 | 250 | PF01048 | 0.560 |
MOD_GlcNHglycan | 273 | 276 | PF01048 | 0.453 |
MOD_GlcNHglycan | 496 | 501 | PF01048 | 0.604 |
MOD_GlcNHglycan | 517 | 520 | PF01048 | 0.577 |
MOD_GlcNHglycan | 57 | 60 | PF01048 | 0.416 |
MOD_GlcNHglycan | 601 | 604 | PF01048 | 0.626 |
MOD_GlcNHglycan | 608 | 611 | PF01048 | 0.594 |
MOD_GlcNHglycan | 620 | 623 | PF01048 | 0.490 |
MOD_GSK3_1 | 109 | 116 | PF00069 | 0.564 |
MOD_GSK3_1 | 136 | 143 | PF00069 | 0.604 |
MOD_GSK3_1 | 218 | 225 | PF00069 | 0.719 |
MOD_GSK3_1 | 229 | 236 | PF00069 | 0.695 |
MOD_GSK3_1 | 248 | 255 | PF00069 | 0.601 |
MOD_GSK3_1 | 267 | 274 | PF00069 | 0.395 |
MOD_GSK3_1 | 358 | 365 | PF00069 | 0.617 |
MOD_GSK3_1 | 423 | 430 | PF00069 | 0.354 |
MOD_GSK3_1 | 442 | 449 | PF00069 | 0.656 |
MOD_GSK3_1 | 459 | 466 | PF00069 | 0.363 |
MOD_GSK3_1 | 496 | 503 | PF00069 | 0.532 |
MOD_GSK3_1 | 515 | 522 | PF00069 | 0.660 |
MOD_GSK3_1 | 598 | 605 | PF00069 | 0.624 |
MOD_GSK3_1 | 623 | 630 | PF00069 | 0.680 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.643 |
MOD_N-GLC_1 | 534 | 539 | PF02516 | 0.486 |
MOD_N-GLC_1 | 598 | 603 | PF02516 | 0.535 |
MOD_N-GLC_1 | 663 | 668 | PF02516 | 0.661 |
MOD_NEK2_1 | 114 | 119 | PF00069 | 0.524 |
MOD_NEK2_1 | 138 | 143 | PF00069 | 0.660 |
MOD_NEK2_1 | 273 | 278 | PF00069 | 0.516 |
MOD_NEK2_1 | 285 | 290 | PF00069 | 0.439 |
MOD_NEK2_1 | 362 | 367 | PF00069 | 0.655 |
MOD_NEK2_1 | 374 | 379 | PF00069 | 0.329 |
MOD_NEK2_1 | 459 | 464 | PF00069 | 0.386 |
MOD_NEK2_1 | 598 | 603 | PF00069 | 0.602 |
MOD_NEK2_2 | 448 | 453 | PF00069 | 0.530 |
MOD_OFUCOSY | 573 | 580 | PF10250 | 0.472 |
MOD_PIKK_1 | 513 | 519 | PF00454 | 0.679 |
MOD_PKA_2 | 267 | 273 | PF00069 | 0.418 |
MOD_PKA_2 | 288 | 294 | PF00069 | 0.416 |
MOD_PKA_2 | 606 | 612 | PF00069 | 0.695 |
MOD_PKA_2 | 651 | 657 | PF00069 | 0.611 |
MOD_PKB_1 | 301 | 309 | PF00069 | 0.462 |
MOD_Plk_2-3 | 358 | 364 | PF00069 | 0.605 |
MOD_Plk_2-3 | 653 | 659 | PF00069 | 0.653 |
MOD_Plk_4 | 10 | 16 | PF00069 | 0.392 |
MOD_Plk_4 | 114 | 120 | PF00069 | 0.524 |
MOD_Plk_4 | 273 | 279 | PF00069 | 0.513 |
MOD_Plk_4 | 423 | 429 | PF00069 | 0.340 |
MOD_Plk_4 | 459 | 465 | PF00069 | 0.364 |
MOD_Plk_4 | 560 | 566 | PF00069 | 0.488 |
MOD_Plk_4 | 60 | 66 | PF00069 | 0.392 |
MOD_Plk_4 | 645 | 651 | PF00069 | 0.574 |
MOD_ProDKin_1 | 109 | 115 | PF00069 | 0.560 |
MOD_ProDKin_1 | 141 | 147 | PF00069 | 0.653 |
MOD_ProDKin_1 | 218 | 224 | PF00069 | 0.708 |
MOD_ProDKin_1 | 233 | 239 | PF00069 | 0.538 |
MOD_ProDKin_1 | 437 | 443 | PF00069 | 0.460 |
MOD_ProDKin_1 | 48 | 54 | PF00069 | 0.420 |
MOD_ProDKin_1 | 602 | 608 | PF00069 | 0.684 |
MOD_ProDKin_1 | 609 | 615 | PF00069 | 0.622 |
MOD_ProDKin_1 | 623 | 629 | PF00069 | 0.467 |
MOD_ProDKin_1 | 84 | 90 | PF00069 | 0.579 |
MOD_ProDKin_1 | 99 | 105 | PF00069 | 0.566 |
TRG_ENDOCYTIC_2 | 269 | 272 | PF00928 | 0.471 |
TRG_ENDOCYTIC_2 | 299 | 302 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 429 | 432 | PF00928 | 0.464 |
TRG_ENDOCYTIC_2 | 467 | 470 | PF00928 | 0.431 |
TRG_ER_diArg_1 | 547 | 549 | PF00400 | 0.553 |
TRG_ER_diArg_1 | 81 | 83 | PF00400 | 0.539 |
TRG_NLS_MonoExtC_3 | 193 | 198 | PF00514 | 0.658 |
TRG_Pf-PMV_PEXEL_1 | 454 | 458 | PF00026 | 0.416 |
TRG_Pf-PMV_PEXEL_1 | 493 | 497 | PF00026 | 0.453 |
TRG_Pf-PMV_PEXEL_1 | 68 | 72 | PF00026 | 0.375 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDC5 | Leptomonas seymouri | 41% | 100% |
A0A3Q8I9K2 | Leishmania donovani | 88% | 100% |
A4H768 | Leishmania braziliensis | 66% | 100% |
A4HVK7 | Leishmania infantum | 88% | 100% |
E9APA3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |