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:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HRG3
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006396 | RNA processing | 6 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0031123 | RNA 3'-end processing | 7 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0071076 | RNA 3' uridylation | 8 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 1 |
GO:0016740 | transferase activity | 2 | 1 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 1 |
GO:0016779 | nucleotidyltransferase activity | 4 | 1 |
GO:0050265 | RNA uridylyltransferase activity | 4 | 1 |
GO:0070569 | uridylyltransferase activity | 5 | 1 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 1 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 177 | 181 | PF00656 | 0.522 |
CLV_NRD_NRD_1 | 132 | 134 | PF00675 | 0.567 |
CLV_NRD_NRD_1 | 229 | 231 | PF00675 | 0.650 |
CLV_NRD_NRD_1 | 265 | 267 | PF00675 | 0.407 |
CLV_NRD_NRD_1 | 342 | 344 | PF00675 | 0.619 |
CLV_NRD_NRD_1 | 356 | 358 | PF00675 | 0.565 |
CLV_NRD_NRD_1 | 420 | 422 | PF00675 | 0.576 |
CLV_NRD_NRD_1 | 425 | 427 | PF00675 | 0.474 |
CLV_NRD_NRD_1 | 444 | 446 | PF00675 | 0.258 |
CLV_NRD_NRD_1 | 472 | 474 | PF00675 | 0.602 |
CLV_NRD_NRD_1 | 502 | 504 | PF00675 | 0.429 |
CLV_NRD_NRD_1 | 598 | 600 | PF00675 | 0.577 |
CLV_NRD_NRD_1 | 8 | 10 | PF00675 | 0.484 |
CLV_PCSK_FUR_1 | 442 | 446 | PF00082 | 0.429 |
CLV_PCSK_KEX2_1 | 132 | 134 | PF00082 | 0.567 |
CLV_PCSK_KEX2_1 | 229 | 231 | PF00082 | 0.650 |
CLV_PCSK_KEX2_1 | 265 | 267 | PF00082 | 0.407 |
CLV_PCSK_KEX2_1 | 342 | 344 | PF00082 | 0.646 |
CLV_PCSK_KEX2_1 | 356 | 358 | PF00082 | 0.592 |
CLV_PCSK_KEX2_1 | 419 | 421 | PF00082 | 0.557 |
CLV_PCSK_KEX2_1 | 425 | 427 | PF00082 | 0.484 |
CLV_PCSK_KEX2_1 | 444 | 446 | PF00082 | 0.361 |
CLV_PCSK_KEX2_1 | 502 | 504 | PF00082 | 0.429 |
CLV_PCSK_KEX2_1 | 597 | 599 | PF00082 | 0.589 |
CLV_PCSK_KEX2_1 | 8 | 10 | PF00082 | 0.484 |
CLV_PCSK_PC7_1 | 225 | 231 | PF00082 | 0.523 |
CLV_PCSK_PC7_1 | 421 | 427 | PF00082 | 0.527 |
CLV_PCSK_SKI1_1 | 364 | 368 | PF00082 | 0.693 |
CLV_PCSK_SKI1_1 | 426 | 430 | PF00082 | 0.579 |
CLV_PCSK_SKI1_1 | 444 | 448 | PF00082 | 0.313 |
CLV_PCSK_SKI1_1 | 508 | 512 | PF00082 | 0.345 |
CLV_PCSK_SKI1_1 | 522 | 526 | PF00082 | 0.357 |
DEG_APCC_DBOX_1 | 443 | 451 | PF00400 | 0.418 |
DEG_APCC_DBOX_1 | 502 | 510 | PF00400 | 0.365 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.494 |
DEG_SPOP_SBC_1 | 157 | 161 | PF00917 | 0.601 |
DEG_SPOP_SBC_1 | 163 | 167 | PF00917 | 0.597 |
DOC_CYCLIN_RxL_1 | 517 | 530 | PF00134 | 0.432 |
DOC_CYCLIN_yCln2_LP_2 | 146 | 152 | PF00134 | 0.606 |
DOC_CYCLIN_yCln2_LP_2 | 185 | 188 | PF00134 | 0.573 |
DOC_CYCLIN_yCln2_LP_2 | 250 | 256 | PF00134 | 0.377 |
DOC_MAPK_gen_1 | 132 | 138 | PF00069 | 0.562 |
DOC_PP1_RVXF_1 | 202 | 209 | PF00149 | 0.600 |
DOC_PP2B_LxvP_1 | 146 | 149 | PF13499 | 0.628 |
DOC_PP2B_LxvP_1 | 185 | 188 | PF13499 | 0.573 |
DOC_PP2B_LxvP_1 | 217 | 220 | PF13499 | 0.443 |
DOC_PP2B_LxvP_1 | 250 | 253 | PF13499 | 0.459 |
DOC_PP2B_LxvP_1 | 369 | 372 | PF13499 | 0.625 |
DOC_PP2B_LxvP_1 | 44 | 47 | PF13499 | 0.482 |
DOC_PP4_FxxP_1 | 208 | 211 | PF00568 | 0.486 |
DOC_USP7_MATH_1 | 153 | 157 | PF00917 | 0.632 |
DOC_USP7_MATH_1 | 162 | 166 | PF00917 | 0.678 |
DOC_USP7_MATH_1 | 28 | 32 | PF00917 | 0.514 |
DOC_USP7_MATH_1 | 318 | 322 | PF00917 | 0.744 |
DOC_USP7_MATH_1 | 341 | 345 | PF00917 | 0.699 |
DOC_USP7_MATH_1 | 375 | 379 | PF00917 | 0.636 |
DOC_USP7_MATH_1 | 382 | 386 | PF00917 | 0.641 |
DOC_USP7_MATH_1 | 428 | 432 | PF00917 | 0.596 |
DOC_USP7_MATH_1 | 437 | 441 | PF00917 | 0.502 |
DOC_USP7_MATH_1 | 446 | 450 | PF00917 | 0.297 |
DOC_USP7_MATH_1 | 465 | 469 | PF00917 | 0.443 |
DOC_USP7_MATH_1 | 92 | 96 | PF00917 | 0.556 |
DOC_WW_Pin1_4 | 136 | 141 | PF00397 | 0.600 |
DOC_WW_Pin1_4 | 42 | 47 | PF00397 | 0.481 |
DOC_WW_Pin1_4 | 433 | 438 | PF00397 | 0.428 |
LIG_14-3-3_CanoR_1 | 132 | 137 | PF00244 | 0.590 |
LIG_14-3-3_CanoR_1 | 426 | 435 | PF00244 | 0.520 |
LIG_14-3-3_CanoR_1 | 493 | 498 | PF00244 | 0.484 |
LIG_BIR_III_4 | 317 | 321 | PF00653 | 0.617 |
LIG_eIF4E_1 | 218 | 224 | PF01652 | 0.453 |
LIG_FHA_1 | 133 | 139 | PF00498 | 0.534 |
LIG_FHA_1 | 169 | 175 | PF00498 | 0.570 |
LIG_FHA_1 | 283 | 289 | PF00498 | 0.482 |
LIG_FHA_1 | 531 | 537 | PF00498 | 0.402 |
LIG_FHA_1 | 569 | 575 | PF00498 | 0.587 |
LIG_FHA_2 | 525 | 531 | PF00498 | 0.382 |
LIG_FHA_2 | 63 | 69 | PF00498 | 0.497 |
LIG_LIR_Apic_2 | 183 | 187 | PF02991 | 0.524 |
LIG_LIR_Nem_3 | 139 | 145 | PF02991 | 0.548 |
LIG_NRBOX | 246 | 252 | PF00104 | 0.370 |
LIG_PCNA_yPIPBox_3 | 225 | 235 | PF02747 | 0.397 |
LIG_SH2_CRK | 218 | 222 | PF00017 | 0.512 |
LIG_SH2_NCK_1 | 111 | 115 | PF00017 | 0.531 |
LIG_SH2_SRC | 218 | 221 | PF00017 | 0.549 |
LIG_SH2_SRC | 482 | 485 | PF00017 | 0.445 |
LIG_SH2_STAP1 | 237 | 241 | PF00017 | 0.388 |
LIG_SH2_STAT5 | 276 | 279 | PF00017 | 0.334 |
LIG_SH2_STAT5 | 455 | 458 | PF00017 | 0.361 |
LIG_SH2_STAT5 | 477 | 480 | PF00017 | 0.436 |
LIG_SH2_STAT5 | 631 | 634 | PF00017 | 0.485 |
LIG_SH3_1 | 481 | 487 | PF00018 | 0.492 |
LIG_SH3_3 | 176 | 182 | PF00018 | 0.572 |
LIG_SH3_3 | 24 | 30 | PF00018 | 0.536 |
LIG_SH3_3 | 330 | 336 | PF00018 | 0.649 |
LIG_SH3_3 | 369 | 375 | PF00018 | 0.629 |
LIG_SH3_3 | 40 | 46 | PF00018 | 0.455 |
LIG_SH3_3 | 459 | 465 | PF00018 | 0.448 |
LIG_SH3_3 | 481 | 487 | PF00018 | 0.492 |
LIG_TRAF2_1 | 387 | 390 | PF00917 | 0.634 |
LIG_UBA3_1 | 626 | 634 | PF00899 | 0.352 |
LIG_WW_3 | 490 | 494 | PF00397 | 0.493 |
MOD_CK1_1 | 156 | 162 | PF00069 | 0.542 |
MOD_CK1_1 | 321 | 327 | PF00069 | 0.759 |
MOD_CK1_1 | 373 | 379 | PF00069 | 0.621 |
MOD_CK1_1 | 427 | 433 | PF00069 | 0.442 |
MOD_CK1_1 | 45 | 51 | PF00069 | 0.488 |
MOD_CK1_1 | 58 | 64 | PF00069 | 0.476 |
MOD_CK1_1 | 94 | 100 | PF00069 | 0.589 |
MOD_CK2_1 | 187 | 193 | PF00069 | 0.619 |
MOD_CK2_1 | 384 | 390 | PF00069 | 0.615 |
MOD_CK2_1 | 465 | 471 | PF00069 | 0.457 |
MOD_CK2_1 | 524 | 530 | PF00069 | 0.405 |
MOD_Cter_Amidation | 130 | 133 | PF01082 | 0.551 |
MOD_GlcNHglycan | 160 | 163 | PF01048 | 0.650 |
MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.607 |
MOD_GlcNHglycan | 316 | 321 | PF01048 | 0.625 |
MOD_GlcNHglycan | 323 | 326 | PF01048 | 0.655 |
MOD_GlcNHglycan | 375 | 378 | PF01048 | 0.686 |
MOD_GlcNHglycan | 394 | 397 | PF01048 | 0.668 |
MOD_GlcNHglycan | 426 | 429 | PF01048 | 0.432 |
MOD_GlcNHglycan | 430 | 433 | PF01048 | 0.393 |
MOD_GlcNHglycan | 457 | 460 | PF01048 | 0.464 |
MOD_GlcNHglycan | 561 | 564 | PF01048 | 0.567 |
MOD_GlcNHglycan | 571 | 574 | PF01048 | 0.592 |
MOD_GSK3_1 | 132 | 139 | PF00069 | 0.645 |
MOD_GSK3_1 | 153 | 160 | PF00069 | 0.622 |
MOD_GSK3_1 | 164 | 171 | PF00069 | 0.604 |
MOD_GSK3_1 | 187 | 194 | PF00069 | 0.631 |
MOD_GSK3_1 | 278 | 285 | PF00069 | 0.409 |
MOD_GSK3_1 | 321 | 328 | PF00069 | 0.729 |
MOD_GSK3_1 | 424 | 431 | PF00069 | 0.509 |
MOD_GSK3_1 | 433 | 440 | PF00069 | 0.402 |
MOD_GSK3_1 | 51 | 58 | PF00069 | 0.503 |
MOD_GSK3_1 | 530 | 537 | PF00069 | 0.403 |
MOD_LATS_1 | 130 | 136 | PF00433 | 0.516 |
MOD_LATS_1 | 591 | 597 | PF00433 | 0.600 |
MOD_N-GLC_1 | 18 | 23 | PF02516 | 0.546 |
MOD_N-GLC_1 | 568 | 573 | PF02516 | 0.603 |
MOD_NEK2_1 | 192 | 197 | PF00069 | 0.545 |
MOD_NEK2_1 | 414 | 419 | PF00069 | 0.577 |
MOD_NEK2_1 | 476 | 481 | PF00069 | 0.386 |
MOD_NEK2_1 | 524 | 529 | PF00069 | 0.366 |
MOD_OFUCOSY | 279 | 286 | PF10250 | 0.373 |
MOD_OFUCOSY | 42 | 49 | PF10250 | 0.485 |
MOD_PIKK_1 | 192 | 198 | PF00454 | 0.558 |
MOD_PIKK_1 | 463 | 469 | PF00454 | 0.507 |
MOD_PIKK_1 | 485 | 491 | PF00454 | 0.411 |
MOD_PKA_1 | 132 | 138 | PF00069 | 0.501 |
MOD_PKA_2 | 132 | 138 | PF00069 | 0.607 |
MOD_PKA_2 | 15 | 21 | PF00069 | 0.544 |
MOD_PKA_2 | 341 | 347 | PF00069 | 0.664 |
MOD_PKA_2 | 349 | 355 | PF00069 | 0.534 |
MOD_PKA_2 | 424 | 430 | PF00069 | 0.468 |
MOD_Plk_1 | 23 | 29 | PF00069 | 0.543 |
MOD_Plk_2-3 | 233 | 239 | PF00069 | 0.393 |
MOD_Plk_4 | 180 | 186 | PF00069 | 0.585 |
MOD_Plk_4 | 242 | 248 | PF00069 | 0.450 |
MOD_Plk_4 | 446 | 452 | PF00069 | 0.486 |
MOD_ProDKin_1 | 136 | 142 | PF00069 | 0.592 |
MOD_ProDKin_1 | 42 | 48 | PF00069 | 0.482 |
MOD_ProDKin_1 | 433 | 439 | PF00069 | 0.423 |
MOD_SUMO_rev_2 | 68 | 73 | PF00179 | 0.472 |
TRG_DiLeu_BaLyEn_6 | 210 | 215 | PF01217 | 0.473 |
TRG_ER_diArg_1 | 120 | 123 | PF00400 | 0.644 |
TRG_ER_diArg_1 | 229 | 231 | PF00400 | 0.595 |
TRG_ER_diArg_1 | 356 | 359 | PF00400 | 0.608 |
TRG_ER_diArg_1 | 410 | 413 | PF00400 | 0.597 |
TRG_ER_diArg_1 | 418 | 421 | PF00400 | 0.520 |
TRG_ER_diArg_1 | 441 | 444 | PF00400 | 0.441 |
TRG_ER_diArg_1 | 501 | 503 | PF00400 | 0.438 |
TRG_ER_diArg_1 | 597 | 599 | PF00400 | 0.592 |
TRG_Pf-PMV_PEXEL_1 | 229 | 233 | PF00026 | 0.461 |
TRG_Pf-PMV_PEXEL_1 | 628 | 633 | PF00026 | 0.476 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IL81 | Leptomonas seymouri | 36% | 100% |
A0A451EJ97 | Leishmania donovani | 99% | 100% |
A4H366 | Leishmania braziliensis | 69% | 100% |
E9AC31 | Leishmania major | 88% | 98% |
E9AJC8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 97% |