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: 8 |
NetGPI | no | yes: 0, no: 8 |
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: A4HJ19
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 9 |
GO:0006396 | RNA processing | 6 | 9 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 9 |
GO:0006807 | nitrogen compound metabolic process | 2 | 9 |
GO:0008152 | metabolic process | 1 | 9 |
GO:0009987 | cellular process | 1 | 9 |
GO:0016070 | RNA metabolic process | 5 | 9 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 9 |
GO:0043170 | macromolecule metabolic process | 3 | 9 |
GO:0044237 | cellular metabolic process | 2 | 9 |
GO:0044238 | primary metabolic process | 2 | 9 |
GO:0046483 | heterocycle metabolic process | 3 | 9 |
GO:0071704 | organic substance metabolic process | 2 | 9 |
GO:0090304 | nucleic acid metabolic process | 4 | 9 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 9 |
GO:0006399 | tRNA metabolic process | 7 | 1 |
GO:0008033 | tRNA processing | 8 | 1 |
GO:0034470 | ncRNA processing | 7 | 1 |
GO:0034660 | ncRNA metabolic process | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 9 |
GO:0003723 | RNA binding | 4 | 9 |
GO:0003824 | catalytic activity | 1 | 9 |
GO:0004000 | adenosine deaminase activity | 4 | 9 |
GO:0005488 | binding | 1 | 9 |
GO:0016787 | hydrolase activity | 2 | 9 |
GO:0016810 | hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds | 3 | 9 |
GO:0016814 | hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in cyclic amidines | 4 | 9 |
GO:0019239 | deaminase activity | 3 | 9 |
GO:0097159 | organic cyclic compound binding | 2 | 9 |
GO:1901363 | heterocyclic compound binding | 2 | 9 |
GO:0008251 | tRNA-specific adenosine deaminase activity | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 147 | 151 | PF00656 | 0.560 |
CLV_C14_Caspase3-7 | 167 | 171 | PF00656 | 0.362 |
CLV_C14_Caspase3-7 | 566 | 570 | PF00656 | 0.486 |
CLV_NRD_NRD_1 | 114 | 116 | PF00675 | 0.551 |
CLV_NRD_NRD_1 | 143 | 145 | PF00675 | 0.370 |
CLV_NRD_NRD_1 | 158 | 160 | PF00675 | 0.221 |
CLV_NRD_NRD_1 | 186 | 188 | PF00675 | 0.323 |
CLV_NRD_NRD_1 | 325 | 327 | PF00675 | 0.301 |
CLV_NRD_NRD_1 | 368 | 370 | PF00675 | 0.618 |
CLV_NRD_NRD_1 | 430 | 432 | PF00675 | 0.685 |
CLV_NRD_NRD_1 | 483 | 485 | PF00675 | 0.694 |
CLV_PCSK_FUR_1 | 366 | 370 | PF00082 | 0.618 |
CLV_PCSK_KEX2_1 | 114 | 116 | PF00082 | 0.551 |
CLV_PCSK_KEX2_1 | 143 | 145 | PF00082 | 0.370 |
CLV_PCSK_KEX2_1 | 158 | 160 | PF00082 | 0.221 |
CLV_PCSK_KEX2_1 | 186 | 188 | PF00082 | 0.364 |
CLV_PCSK_KEX2_1 | 324 | 326 | PF00082 | 0.301 |
CLV_PCSK_KEX2_1 | 368 | 370 | PF00082 | 0.642 |
CLV_PCSK_KEX2_1 | 432 | 434 | PF00082 | 0.645 |
CLV_PCSK_KEX2_1 | 483 | 485 | PF00082 | 0.694 |
CLV_PCSK_PC1ET2_1 | 432 | 434 | PF00082 | 0.645 |
CLV_PCSK_PC7_1 | 479 | 485 | PF00082 | 0.707 |
CLV_PCSK_SKI1_1 | 143 | 147 | PF00082 | 0.399 |
CLV_PCSK_SKI1_1 | 274 | 278 | PF00082 | 0.294 |
CLV_PCSK_SKI1_1 | 398 | 402 | PF00082 | 0.574 |
DEG_APCC_DBOX_1 | 325 | 333 | PF00400 | 0.465 |
DEG_APCC_KENBOX_2 | 514 | 518 | PF00400 | 0.466 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.792 |
DEG_SCF_TRCP1_1 | 413 | 419 | PF00400 | 0.546 |
DEG_SPOP_SBC_1 | 6 | 10 | PF00917 | 0.504 |
DOC_ANK_TNKS_1 | 186 | 193 | PF00023 | 0.406 |
DOC_CDC14_PxL_1 | 17 | 25 | PF14671 | 0.358 |
DOC_CYCLIN_RxL_1 | 140 | 150 | PF00134 | 0.596 |
DOC_MAPK_DCC_7 | 324 | 334 | PF00069 | 0.528 |
DOC_MAPK_gen_1 | 114 | 121 | PF00069 | 0.492 |
DOC_MAPK_gen_1 | 158 | 164 | PF00069 | 0.448 |
DOC_MAPK_gen_1 | 312 | 321 | PF00069 | 0.501 |
DOC_MAPK_MEF2A_6 | 114 | 121 | PF00069 | 0.434 |
DOC_MAPK_MEF2A_6 | 209 | 216 | PF00069 | 0.430 |
DOC_MAPK_MEF2A_6 | 506 | 513 | PF00069 | 0.412 |
DOC_MAPK_NFAT4_5 | 506 | 514 | PF00069 | 0.416 |
DOC_PP1_RVXF_1 | 572 | 578 | PF00149 | 0.714 |
DOC_PP2B_LxvP_1 | 89 | 92 | PF13499 | 0.413 |
DOC_PP4_FxxP_1 | 330 | 333 | PF00568 | 0.501 |
DOC_USP7_MATH_1 | 104 | 108 | PF00917 | 0.576 |
DOC_USP7_MATH_1 | 109 | 113 | PF00917 | 0.471 |
DOC_USP7_MATH_1 | 169 | 173 | PF00917 | 0.568 |
DOC_USP7_MATH_1 | 198 | 202 | PF00917 | 0.406 |
DOC_USP7_MATH_1 | 230 | 234 | PF00917 | 0.566 |
DOC_USP7_MATH_1 | 402 | 406 | PF00917 | 0.755 |
DOC_USP7_MATH_1 | 439 | 443 | PF00917 | 0.675 |
DOC_USP7_MATH_1 | 529 | 533 | PF00917 | 0.715 |
DOC_USP7_MATH_1 | 59 | 63 | PF00917 | 0.702 |
DOC_USP7_MATH_1 | 590 | 594 | PF00917 | 0.566 |
DOC_USP7_MATH_1 | 6 | 10 | PF00917 | 0.545 |
DOC_USP7_MATH_1 | 66 | 70 | PF00917 | 0.715 |
DOC_WW_Pin1_4 | 24 | 29 | PF00397 | 0.542 |
DOC_WW_Pin1_4 | 540 | 545 | PF00397 | 0.609 |
LIG_14-3-3_CanoR_1 | 264 | 270 | PF00244 | 0.436 |
LIG_14-3-3_CanoR_1 | 324 | 330 | PF00244 | 0.534 |
LIG_14-3-3_CanoR_1 | 368 | 378 | PF00244 | 0.484 |
LIG_14-3-3_CanoR_1 | 483 | 489 | PF00244 | 0.714 |
LIG_Actin_WH2_2 | 193 | 211 | PF00022 | 0.406 |
LIG_BRCT_BRCA1_1 | 89 | 93 | PF00533 | 0.253 |
LIG_deltaCOP1_diTrp_1 | 311 | 316 | PF00928 | 0.560 |
LIG_EH1_1 | 504 | 512 | PF00400 | 0.406 |
LIG_FHA_1 | 209 | 215 | PF00498 | 0.564 |
LIG_FHA_1 | 250 | 256 | PF00498 | 0.406 |
LIG_FHA_1 | 286 | 292 | PF00498 | 0.488 |
LIG_FHA_1 | 308 | 314 | PF00498 | 0.537 |
LIG_FHA_2 | 454 | 460 | PF00498 | 0.520 |
LIG_FHA_2 | 485 | 491 | PF00498 | 0.663 |
LIG_FHA_2 | 543 | 549 | PF00498 | 0.494 |
LIG_FHA_2 | 566 | 572 | PF00498 | 0.744 |
LIG_FHA_2 | 6 | 12 | PF00498 | 0.768 |
LIG_LIR_Apic_2 | 328 | 333 | PF02991 | 0.500 |
LIG_LIR_Apic_2 | 448 | 454 | PF02991 | 0.489 |
LIG_LIR_Gen_1 | 279 | 287 | PF02991 | 0.406 |
LIG_LIR_Gen_1 | 344 | 352 | PF02991 | 0.406 |
LIG_LIR_Gen_1 | 419 | 428 | PF02991 | 0.682 |
LIG_LIR_Nem_3 | 279 | 284 | PF02991 | 0.406 |
LIG_LIR_Nem_3 | 344 | 349 | PF02991 | 0.522 |
LIG_LIR_Nem_3 | 419 | 424 | PF02991 | 0.718 |
LIG_LIR_Nem_3 | 442 | 447 | PF02991 | 0.773 |
LIG_RPA_C_Fungi | 154 | 166 | PF08784 | 0.253 |
LIG_SH2_CRK | 281 | 285 | PF00017 | 0.491 |
LIG_SH2_NCK_1 | 533 | 537 | PF00017 | 0.772 |
LIG_SH2_PTP2 | 116 | 119 | PF00017 | 0.529 |
LIG_SH2_SRC | 533 | 536 | PF00017 | 0.506 |
LIG_SH2_STAP1 | 180 | 184 | PF00017 | 0.491 |
LIG_SH2_STAT3 | 561 | 564 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 116 | 119 | PF00017 | 0.476 |
LIG_SH3_3 | 375 | 381 | PF00018 | 0.656 |
LIG_SxIP_EBH_1 | 483 | 497 | PF03271 | 0.481 |
LIG_TRAF2_1 | 69 | 72 | PF00917 | 0.629 |
LIG_UBA3_1 | 509 | 515 | PF00899 | 0.428 |
MOD_CK1_1 | 120 | 126 | PF00069 | 0.369 |
MOD_CK1_1 | 233 | 239 | PF00069 | 0.405 |
MOD_CK1_1 | 267 | 273 | PF00069 | 0.335 |
MOD_CK1_1 | 387 | 393 | PF00069 | 0.483 |
MOD_CK1_1 | 411 | 417 | PF00069 | 0.687 |
MOD_CK1_1 | 486 | 492 | PF00069 | 0.593 |
MOD_CK1_1 | 523 | 529 | PF00069 | 0.652 |
MOD_CK1_1 | 542 | 548 | PF00069 | 0.635 |
MOD_CK1_1 | 7 | 13 | PF00069 | 0.493 |
MOD_CK2_1 | 369 | 375 | PF00069 | 0.646 |
MOD_CK2_1 | 387 | 393 | PF00069 | 0.320 |
MOD_CK2_1 | 431 | 437 | PF00069 | 0.775 |
MOD_CK2_1 | 484 | 490 | PF00069 | 0.713 |
MOD_CK2_1 | 5 | 11 | PF00069 | 0.765 |
MOD_CK2_1 | 534 | 540 | PF00069 | 0.620 |
MOD_CK2_1 | 66 | 72 | PF00069 | 0.668 |
MOD_Cter_Amidation | 322 | 325 | PF01082 | 0.357 |
MOD_GlcNHglycan | 106 | 110 | PF01048 | 0.593 |
MOD_GlcNHglycan | 122 | 125 | PF01048 | 0.302 |
MOD_GlcNHglycan | 170 | 174 | PF01048 | 0.491 |
MOD_GlcNHglycan | 232 | 235 | PF01048 | 0.388 |
MOD_GlcNHglycan | 389 | 392 | PF01048 | 0.538 |
MOD_GlcNHglycan | 413 | 416 | PF01048 | 0.574 |
MOD_GlcNHglycan | 440 | 444 | PF01048 | 0.684 |
MOD_GlcNHglycan | 529 | 532 | PF01048 | 0.746 |
MOD_GlcNHglycan | 565 | 568 | PF01048 | 0.723 |
MOD_GlcNHglycan | 72 | 76 | PF01048 | 0.636 |
MOD_GSK3_1 | 105 | 112 | PF00069 | 0.429 |
MOD_GSK3_1 | 169 | 176 | PF00069 | 0.503 |
MOD_GSK3_1 | 229 | 236 | PF00069 | 0.435 |
MOD_GSK3_1 | 263 | 270 | PF00069 | 0.475 |
MOD_GSK3_1 | 276 | 283 | PF00069 | 0.224 |
MOD_GSK3_1 | 303 | 310 | PF00069 | 0.438 |
MOD_GSK3_1 | 394 | 401 | PF00069 | 0.459 |
MOD_GSK3_1 | 439 | 446 | PF00069 | 0.697 |
MOD_GSK3_1 | 523 | 530 | PF00069 | 0.721 |
MOD_GSK3_1 | 540 | 547 | PF00069 | 0.605 |
MOD_GSK3_1 | 565 | 572 | PF00069 | 0.747 |
MOD_GSK3_1 | 590 | 597 | PF00069 | 0.493 |
MOD_N-GLC_1 | 303 | 308 | PF02516 | 0.438 |
MOD_N-GLC_1 | 411 | 416 | PF02516 | 0.627 |
MOD_NEK2_1 | 208 | 213 | PF00069 | 0.486 |
MOD_NEK2_1 | 216 | 221 | PF00069 | 0.398 |
MOD_NEK2_1 | 222 | 227 | PF00069 | 0.363 |
MOD_NEK2_1 | 305 | 310 | PF00069 | 0.357 |
MOD_NEK2_1 | 342 | 347 | PF00069 | 0.445 |
MOD_NEK2_1 | 394 | 399 | PF00069 | 0.555 |
MOD_NEK2_1 | 422 | 427 | PF00069 | 0.480 |
MOD_NEK2_1 | 552 | 557 | PF00069 | 0.644 |
MOD_NEK2_1 | 563 | 568 | PF00069 | 0.408 |
MOD_NEK2_1 | 576 | 581 | PF00069 | 0.642 |
MOD_NEK2_1 | 87 | 92 | PF00069 | 0.450 |
MOD_NEK2_2 | 109 | 114 | PF00069 | 0.379 |
MOD_NEK2_2 | 384 | 389 | PF00069 | 0.293 |
MOD_NEK2_2 | 590 | 595 | PF00069 | 0.489 |
MOD_PIKK_1 | 285 | 291 | PF00454 | 0.224 |
MOD_PIKK_1 | 552 | 558 | PF00454 | 0.663 |
MOD_PIKK_1 | 577 | 583 | PF00454 | 0.448 |
MOD_PK_1 | 335 | 341 | PF00069 | 0.363 |
MOD_PKA_1 | 325 | 331 | PF00069 | 0.347 |
MOD_PKA_1 | 431 | 437 | PF00069 | 0.510 |
MOD_PKA_1 | 483 | 489 | PF00069 | 0.714 |
MOD_PKA_2 | 173 | 179 | PF00069 | 0.435 |
MOD_PKA_2 | 208 | 214 | PF00069 | 0.491 |
MOD_PKA_2 | 263 | 269 | PF00069 | 0.423 |
MOD_PKA_2 | 325 | 331 | PF00069 | 0.340 |
MOD_PKA_2 | 483 | 489 | PF00069 | 0.714 |
MOD_Plk_1 | 109 | 115 | PF00069 | 0.363 |
MOD_Plk_1 | 249 | 255 | PF00069 | 0.224 |
MOD_Plk_1 | 303 | 309 | PF00069 | 0.438 |
MOD_Plk_1 | 439 | 445 | PF00069 | 0.510 |
MOD_Plk_1 | 550 | 556 | PF00069 | 0.705 |
MOD_Plk_4 | 325 | 331 | PF00069 | 0.310 |
MOD_Plk_4 | 423 | 429 | PF00069 | 0.483 |
MOD_Plk_4 | 460 | 466 | PF00069 | 0.668 |
MOD_Plk_4 | 534 | 540 | PF00069 | 0.641 |
MOD_ProDKin_1 | 24 | 30 | PF00069 | 0.542 |
MOD_ProDKin_1 | 540 | 546 | PF00069 | 0.608 |
MOD_SUMO_for_1 | 204 | 207 | PF00179 | 0.224 |
MOD_SUMO_rev_2 | 425 | 434 | PF00179 | 0.728 |
TRG_DiLeu_BaLyEn_6 | 571 | 576 | PF01217 | 0.624 |
TRG_ENDOCYTIC_2 | 116 | 119 | PF00928 | 0.460 |
TRG_ENDOCYTIC_2 | 180 | 183 | PF00928 | 0.438 |
TRG_ENDOCYTIC_2 | 281 | 284 | PF00928 | 0.385 |
TRG_ER_diArg_1 | 113 | 115 | PF00400 | 0.574 |
TRG_ER_diArg_1 | 142 | 144 | PF00400 | 0.485 |
TRG_ER_diArg_1 | 185 | 187 | PF00400 | 0.491 |
TRG_ER_diArg_1 | 324 | 326 | PF00400 | 0.357 |
TRG_ER_diArg_1 | 365 | 368 | PF00400 | 0.576 |
TRG_ER_diArg_1 | 418 | 421 | PF00400 | 0.657 |
TRG_ER_diArg_1 | 482 | 484 | PF00400 | 0.453 |
TRG_Pf-PMV_PEXEL_1 | 126 | 131 | PF00026 | 0.264 |
TRG_Pf-PMV_PEXEL_1 | 143 | 147 | PF00026 | 0.439 |
TRG_Pf-PMV_PEXEL_1 | 45 | 49 | PF00026 | 0.534 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P680 | Leptomonas seymouri | 42% | 100% |
A0A3Q8IGD9 | Leishmania donovani | 71% | 100% |
A0A422NGA7 | Trypanosoma rangeli | 32% | 98% |
A4I8P1 | Leishmania infantum | 71% | 100% |
D0A4L8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 97% |
E9B3K2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 71% | 100% |
Q4Q4J9 | Leishmania major | 70% | 100% |