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: A4H366
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 | 501 | 505 | PF00656 | 0.503 |
CLV_NRD_NRD_1 | 170 | 172 | PF00675 | 0.653 |
CLV_NRD_NRD_1 | 206 | 208 | PF00675 | 0.400 |
CLV_NRD_NRD_1 | 296 | 298 | PF00675 | 0.589 |
CLV_NRD_NRD_1 | 352 | 354 | PF00675 | 0.529 |
CLV_NRD_NRD_1 | 360 | 362 | PF00675 | 0.564 |
CLV_NRD_NRD_1 | 365 | 367 | PF00675 | 0.445 |
CLV_NRD_NRD_1 | 384 | 386 | PF00675 | 0.266 |
CLV_NRD_NRD_1 | 412 | 414 | PF00675 | 0.604 |
CLV_PCSK_FUR_1 | 382 | 386 | PF00082 | 0.434 |
CLV_PCSK_KEX2_1 | 170 | 172 | PF00082 | 0.653 |
CLV_PCSK_KEX2_1 | 206 | 208 | PF00082 | 0.400 |
CLV_PCSK_KEX2_1 | 296 | 298 | PF00082 | 0.616 |
CLV_PCSK_KEX2_1 | 352 | 354 | PF00082 | 0.534 |
CLV_PCSK_KEX2_1 | 359 | 361 | PF00082 | 0.552 |
CLV_PCSK_KEX2_1 | 365 | 367 | PF00082 | 0.454 |
CLV_PCSK_KEX2_1 | 384 | 386 | PF00082 | 0.369 |
CLV_PCSK_KEX2_1 | 412 | 414 | PF00082 | 0.471 |
CLV_PCSK_PC7_1 | 361 | 367 | PF00082 | 0.504 |
CLV_PCSK_SKI1_1 | 304 | 308 | PF00082 | 0.696 |
CLV_PCSK_SKI1_1 | 366 | 370 | PF00082 | 0.551 |
CLV_PCSK_SKI1_1 | 384 | 388 | PF00082 | 0.318 |
CLV_PCSK_SKI1_1 | 462 | 466 | PF00082 | 0.339 |
CLV_PCSK_SKI1_1 | 74 | 78 | PF00082 | 0.474 |
DEG_APCC_DBOX_1 | 383 | 391 | PF00400 | 0.422 |
DEG_APCC_DBOX_1 | 442 | 450 | PF00400 | 0.369 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.564 |
DEG_SPOP_SBC_1 | 265 | 269 | PF00917 | 0.527 |
DEG_SPOP_SBC_1 | 368 | 372 | PF00917 | 0.338 |
DOC_CKS1_1 | 509 | 514 | PF01111 | 0.535 |
DOC_CYCLIN_RxL_1 | 142 | 151 | PF00134 | 0.372 |
DOC_CYCLIN_RxL_1 | 459 | 467 | PF00134 | 0.405 |
DOC_CYCLIN_yCln2_LP_2 | 116 | 119 | PF00134 | 0.567 |
DOC_CYCLIN_yCln2_LP_2 | 191 | 197 | PF00134 | 0.392 |
DOC_CYCLIN_yCln2_LP_2 | 466 | 472 | PF00134 | 0.375 |
DOC_CYCLIN_yCln2_LP_2 | 77 | 83 | PF00134 | 0.628 |
DOC_MAPK_gen_1 | 412 | 418 | PF00069 | 0.334 |
DOC_MAPK_MEF2A_6 | 421 | 428 | PF00069 | 0.346 |
DOC_PP1_RVXF_1 | 143 | 150 | PF00149 | 0.520 |
DOC_PP2B_LxvP_1 | 116 | 119 | PF13499 | 0.567 |
DOC_PP2B_LxvP_1 | 158 | 161 | PF13499 | 0.514 |
DOC_PP2B_LxvP_1 | 191 | 194 | PF13499 | 0.474 |
DOC_PP2B_LxvP_1 | 77 | 80 | PF13499 | 0.645 |
DOC_PP4_FxxP_1 | 149 | 152 | PF00568 | 0.457 |
DOC_USP7_MATH_1 | 23 | 27 | PF00917 | 0.542 |
DOC_USP7_MATH_1 | 281 | 285 | PF00917 | 0.671 |
DOC_USP7_MATH_1 | 315 | 319 | PF00917 | 0.647 |
DOC_USP7_MATH_1 | 368 | 372 | PF00917 | 0.573 |
DOC_USP7_MATH_1 | 377 | 381 | PF00917 | 0.498 |
DOC_USP7_MATH_1 | 399 | 403 | PF00917 | 0.455 |
DOC_USP7_MATH_1 | 500 | 504 | PF00917 | 0.541 |
DOC_USP7_MATH_1 | 93 | 97 | PF00917 | 0.762 |
DOC_WW_Pin1_4 | 148 | 153 | PF00397 | 0.375 |
DOC_WW_Pin1_4 | 316 | 321 | PF00397 | 0.547 |
DOC_WW_Pin1_4 | 373 | 378 | PF00397 | 0.415 |
DOC_WW_Pin1_4 | 508 | 513 | PF00397 | 0.622 |
LIG_14-3-3_CanoR_1 | 109 | 115 | PF00244 | 0.508 |
LIG_14-3-3_CanoR_1 | 310 | 315 | PF00244 | 0.531 |
LIG_14-3-3_CanoR_1 | 366 | 375 | PF00244 | 0.497 |
LIG_14-3-3_CanoR_1 | 38 | 44 | PF00244 | 0.387 |
LIG_14-3-3_CanoR_1 | 68 | 76 | PF00244 | 0.548 |
LIG_14-3-3_CanoR_1 | 92 | 101 | PF00244 | 0.510 |
LIG_APCC_ABBA_1 | 492 | 497 | PF00400 | 0.380 |
LIG_eIF4E_1 | 159 | 165 | PF01652 | 0.477 |
LIG_FHA_1 | 187 | 193 | PF00498 | 0.362 |
LIG_FHA_1 | 224 | 230 | PF00498 | 0.486 |
LIG_FHA_1 | 256 | 262 | PF00498 | 0.548 |
LIG_FHA_1 | 370 | 376 | PF00498 | 0.336 |
LIG_FHA_1 | 471 | 477 | PF00498 | 0.377 |
LIG_FHA_1 | 480 | 486 | PF00498 | 0.396 |
LIG_FHA_1 | 83 | 89 | PF00498 | 0.607 |
LIG_FHA_2 | 270 | 276 | PF00498 | 0.538 |
LIG_FHA_2 | 38 | 44 | PF00498 | 0.426 |
LIG_FHA_2 | 499 | 505 | PF00498 | 0.503 |
LIG_FHA_2 | 51 | 57 | PF00498 | 0.425 |
LIG_LIR_Apic_2 | 508 | 512 | PF02991 | 0.535 |
LIG_LIR_Nem_3 | 142 | 147 | PF02991 | 0.429 |
LIG_LIR_Nem_3 | 70 | 76 | PF02991 | 0.547 |
LIG_NRBOX | 187 | 193 | PF00104 | 0.383 |
LIG_Pex14_1 | 57 | 61 | PF04695 | 0.492 |
LIG_PTB_Apo_2 | 250 | 257 | PF02174 | 0.530 |
LIG_PTB_Phospho_1 | 250 | 256 | PF10480 | 0.534 |
LIG_SH2_CRK | 144 | 148 | PF00017 | 0.402 |
LIG_SH2_CRK | 159 | 163 | PF00017 | 0.539 |
LIG_SH2_CRK | 509 | 513 | PF00017 | 0.535 |
LIG_SH2_NCK_1 | 42 | 46 | PF00017 | 0.524 |
LIG_SH2_NCK_1 | 509 | 513 | PF00017 | 0.535 |
LIG_SH2_SRC | 159 | 162 | PF00017 | 0.578 |
LIG_SH2_STAP1 | 178 | 182 | PF00017 | 0.394 |
LIG_SH2_STAP1 | 256 | 260 | PF00017 | 0.517 |
LIG_SH2_STAP1 | 42 | 46 | PF00017 | 0.367 |
LIG_SH2_STAT5 | 217 | 220 | PF00017 | 0.334 |
LIG_SH2_STAT5 | 362 | 365 | PF00017 | 0.410 |
LIG_SH2_STAT5 | 395 | 398 | PF00017 | 0.361 |
LIG_SH2_STAT5 | 417 | 420 | PF00017 | 0.440 |
LIG_SH2_STAT5 | 509 | 512 | PF00017 | 0.535 |
LIG_SH2_STAT5 | 570 | 573 | PF00017 | 0.506 |
LIG_SH3_1 | 421 | 427 | PF00018 | 0.500 |
LIG_SH3_3 | 421 | 427 | PF00018 | 0.503 |
LIG_SH3_3 | 522 | 528 | PF00018 | 0.639 |
LIG_SH3_3 | 73 | 79 | PF00018 | 0.479 |
LIG_SUMO_SIM_anti_2 | 113 | 118 | PF11976 | 0.503 |
MOD_CDC14_SPxK_1 | 151 | 154 | PF00782 | 0.422 |
MOD_CDK_SPxK_1 | 148 | 154 | PF00069 | 0.384 |
MOD_CK1_1 | 186 | 192 | PF00069 | 0.297 |
MOD_CK1_1 | 25 | 31 | PF00069 | 0.585 |
MOD_CK1_1 | 264 | 270 | PF00069 | 0.701 |
MOD_CK1_1 | 316 | 322 | PF00069 | 0.620 |
MOD_CK1_1 | 508 | 514 | PF00069 | 0.561 |
MOD_GlcNHglycan | 263 | 266 | PF01048 | 0.650 |
MOD_GlcNHglycan | 315 | 318 | PF01048 | 0.697 |
MOD_GlcNHglycan | 341 | 344 | PF01048 | 0.580 |
MOD_GlcNHglycan | 397 | 400 | PF01048 | 0.461 |
MOD_GlcNHglycan | 456 | 459 | PF01048 | 0.265 |
MOD_GSK3_1 | 118 | 125 | PF00069 | 0.593 |
MOD_GSK3_1 | 219 | 226 | PF00069 | 0.412 |
MOD_GSK3_1 | 261 | 268 | PF00069 | 0.720 |
MOD_GSK3_1 | 271 | 278 | PF00069 | 0.544 |
MOD_GSK3_1 | 369 | 376 | PF00069 | 0.404 |
MOD_GSK3_1 | 395 | 402 | PF00069 | 0.312 |
MOD_GSK3_1 | 470 | 477 | PF00069 | 0.363 |
MOD_GSK3_1 | 495 | 502 | PF00069 | 0.537 |
MOD_GSK3_1 | 99 | 106 | PF00069 | 0.657 |
MOD_NEK2_1 | 147 | 152 | PF00069 | 0.385 |
MOD_NEK2_1 | 44 | 49 | PF00069 | 0.383 |
MOD_NEK2_1 | 464 | 469 | PF00069 | 0.358 |
MOD_NEK2_1 | 495 | 500 | PF00069 | 0.551 |
MOD_OFUCOSY | 220 | 227 | PF10250 | 0.375 |
MOD_PIKK_1 | 37 | 43 | PF00454 | 0.387 |
MOD_PIKK_1 | 403 | 409 | PF00454 | 0.496 |
MOD_PK_1 | 103 | 109 | PF00069 | 0.499 |
MOD_PKA_2 | 275 | 281 | PF00069 | 0.658 |
MOD_PKA_2 | 289 | 295 | PF00069 | 0.543 |
MOD_PKA_2 | 298 | 304 | PF00069 | 0.552 |
MOD_PKA_2 | 37 | 43 | PF00069 | 0.387 |
MOD_PKA_2 | 67 | 73 | PF00069 | 0.591 |
MOD_PKB_1 | 359 | 367 | PF00069 | 0.363 |
MOD_Plk_2-3 | 174 | 180 | PF00069 | 0.408 |
MOD_Plk_4 | 103 | 109 | PF00069 | 0.560 |
MOD_Plk_4 | 112 | 118 | PF00069 | 0.587 |
MOD_Plk_4 | 183 | 189 | PF00069 | 0.459 |
MOD_Plk_4 | 256 | 262 | PF00069 | 0.518 |
MOD_Plk_4 | 298 | 304 | PF00069 | 0.532 |
MOD_Plk_4 | 332 | 338 | PF00069 | 0.553 |
MOD_ProDKin_1 | 148 | 154 | PF00069 | 0.384 |
MOD_ProDKin_1 | 316 | 322 | PF00069 | 0.549 |
MOD_ProDKin_1 | 373 | 379 | PF00069 | 0.411 |
MOD_ProDKin_1 | 508 | 514 | PF00069 | 0.623 |
TRG_ENDOCYTIC_2 | 144 | 147 | PF00928 | 0.375 |
TRG_ER_diArg_1 | 296 | 299 | PF00400 | 0.636 |
TRG_ER_diArg_1 | 352 | 354 | PF00400 | 0.560 |
TRG_ER_diArg_1 | 358 | 361 | PF00400 | 0.514 |
TRG_ER_diArg_1 | 381 | 384 | PF00400 | 0.450 |
TRG_Pf-PMV_PEXEL_1 | 352 | 357 | PF00026 | 0.439 |
TRG_Pf-PMV_PEXEL_1 | 567 | 572 | PF00026 | 0.487 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IL81 | Leptomonas seymouri | 40% | 97% |
A0A451EJ97 | Leishmania donovani | 69% | 100% |
A4HRG3 | Leishmania infantum | 69% | 90% |
E9AC31 | Leishmania major | 67% | 97% |
E9AJC8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 67% | 100% |