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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 14 |
NetGPI | no | yes: 0, no: 14 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005730 | nucleolus | 5 | 12 |
GO:0043226 | organelle | 2 | 12 |
GO:0043228 | non-membrane-bounded organelle | 3 | 12 |
GO:0043229 | intracellular organelle | 3 | 12 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 13 |
GO:0031974 | membrane-enclosed lumen | 2 | 1 |
GO:0031981 | nuclear lumen | 5 | 1 |
GO:0043233 | organelle lumen | 3 | 1 |
GO:0070013 | intracellular organelle lumen | 4 | 1 |
Related structures:
AlphaFold database: A4HIZ4
Term | Name | Level | Count |
---|---|---|---|
GO:0001510 | RNA methylation | 4 | 15 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 15 |
GO:0006396 | RNA processing | 6 | 12 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 15 |
GO:0006807 | nitrogen compound metabolic process | 2 | 15 |
GO:0008152 | metabolic process | 1 | 15 |
GO:0009451 | RNA modification | 5 | 15 |
GO:0009987 | cellular process | 1 | 15 |
GO:0016070 | RNA metabolic process | 5 | 15 |
GO:0022613 | ribonucleoprotein complex biogenesis | 4 | 11 |
GO:0032259 | methylation | 2 | 15 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 15 |
GO:0042254 | ribosome biogenesis | 5 | 11 |
GO:0043170 | macromolecule metabolic process | 3 | 15 |
GO:0043412 | macromolecule modification | 4 | 15 |
GO:0043414 | macromolecule methylation | 3 | 15 |
GO:0044085 | cellular component biogenesis | 3 | 11 |
GO:0044237 | cellular metabolic process | 2 | 15 |
GO:0044238 | primary metabolic process | 2 | 15 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 15 |
GO:0046483 | heterocycle metabolic process | 3 | 15 |
GO:0071704 | organic substance metabolic process | 2 | 15 |
GO:0071840 | cellular component organization or biogenesis | 2 | 11 |
GO:0090304 | nucleic acid metabolic process | 4 | 15 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 15 |
GO:0000154 | rRNA modification | 6 | 1 |
GO:0000470 | maturation of LSU-rRNA | 9 | 1 |
GO:0006364 | rRNA processing | 8 | 1 |
GO:0016072 | rRNA metabolic process | 7 | 1 |
GO:0031167 | rRNA methylation | 5 | 1 |
GO:0034470 | ncRNA processing | 7 | 1 |
GO:0034660 | ncRNA metabolic process | 6 | 1 |
GO:0070475 | rRNA base methylation | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 15 |
GO:0003723 | RNA binding | 4 | 15 |
GO:0003824 | catalytic activity | 1 | 15 |
GO:0005488 | binding | 1 | 15 |
GO:0008168 | methyltransferase activity | 4 | 15 |
GO:0008757 | S-adenosylmethionine-dependent methyltransferase activity | 5 | 12 |
GO:0016740 | transferase activity | 2 | 15 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 15 |
GO:0097159 | organic cyclic compound binding | 2 | 15 |
GO:1901363 | heterocyclic compound binding | 2 | 15 |
GO:0008169 | C-methyltransferase activity | 5 | 1 |
GO:0008173 | RNA methyltransferase activity | 4 | 1 |
GO:0008649 | rRNA methyltransferase activity | 5 | 1 |
GO:0009383 | rRNA (cytosine-C5-)-methyltransferase activity | 6 | 1 |
GO:0016434 | rRNA (cytosine) methyltransferase activity | 6 | 1 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 1 |
GO:0140102 | catalytic activity, acting on a rRNA | 4 | 1 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 441 | 445 | PF00656 | 0.442 |
CLV_C14_Caspase3-7 | 65 | 69 | PF00656 | 0.513 |
CLV_NRD_NRD_1 | 124 | 126 | PF00675 | 0.479 |
CLV_NRD_NRD_1 | 265 | 267 | PF00675 | 0.225 |
CLV_NRD_NRD_1 | 41 | 43 | PF00675 | 0.542 |
CLV_NRD_NRD_1 | 474 | 476 | PF00675 | 0.233 |
CLV_NRD_NRD_1 | 507 | 509 | PF00675 | 0.243 |
CLV_NRD_NRD_1 | 609 | 611 | PF00675 | 0.650 |
CLV_NRD_NRD_1 | 620 | 622 | PF00675 | 0.613 |
CLV_PCSK_KEX2_1 | 123 | 125 | PF00082 | 0.471 |
CLV_PCSK_KEX2_1 | 264 | 266 | PF00082 | 0.225 |
CLV_PCSK_KEX2_1 | 274 | 276 | PF00082 | 0.253 |
CLV_PCSK_KEX2_1 | 473 | 475 | PF00082 | 0.236 |
CLV_PCSK_KEX2_1 | 507 | 509 | PF00082 | 0.243 |
CLV_PCSK_KEX2_1 | 555 | 557 | PF00082 | 0.654 |
CLV_PCSK_KEX2_1 | 609 | 611 | PF00082 | 0.697 |
CLV_PCSK_PC1ET2_1 | 264 | 266 | PF00082 | 0.225 |
CLV_PCSK_PC1ET2_1 | 274 | 276 | PF00082 | 0.253 |
CLV_PCSK_PC1ET2_1 | 473 | 475 | PF00082 | 0.246 |
CLV_PCSK_PC1ET2_1 | 555 | 557 | PF00082 | 0.706 |
CLV_PCSK_SKI1_1 | 124 | 128 | PF00082 | 0.456 |
CLV_PCSK_SKI1_1 | 144 | 148 | PF00082 | 0.425 |
CLV_PCSK_SKI1_1 | 19 | 23 | PF00082 | 0.543 |
CLV_PCSK_SKI1_1 | 3 | 7 | PF00082 | 0.604 |
CLV_PCSK_SKI1_1 | 400 | 404 | PF00082 | 0.236 |
CLV_PCSK_SKI1_1 | 417 | 421 | PF00082 | 0.236 |
CLV_PCSK_SKI1_1 | 42 | 46 | PF00082 | 0.613 |
CLV_PCSK_SKI1_1 | 436 | 440 | PF00082 | 0.269 |
CLV_Separin_Metazoa | 212 | 216 | PF03568 | 0.431 |
DEG_APCC_DBOX_1 | 214 | 222 | PF00400 | 0.407 |
DEG_ODPH_VHL_1 | 324 | 335 | PF01847 | 0.425 |
DEG_SCF_SKP2-CKS1_1 | 583 | 590 | PF00560 | 0.502 |
DEG_SPOP_SBC_1 | 545 | 549 | PF00917 | 0.661 |
DOC_CYCLIN_RxL_1 | 430 | 444 | PF00134 | 0.449 |
DOC_CYCLIN_yCln2_LP_2 | 235 | 241 | PF00134 | 0.449 |
DOC_MAPK_gen_1 | 184 | 193 | PF00069 | 0.374 |
DOC_MAPK_gen_1 | 205 | 213 | PF00069 | 0.385 |
DOC_MAPK_gen_1 | 250 | 258 | PF00069 | 0.436 |
DOC_MAPK_gen_1 | 284 | 292 | PF00069 | 0.425 |
DOC_MAPK_gen_1 | 393 | 403 | PF00069 | 0.425 |
DOC_MAPK_gen_1 | 473 | 479 | PF00069 | 0.449 |
DOC_MAPK_gen_1 | 495 | 505 | PF00069 | 0.527 |
DOC_MAPK_MEF2A_6 | 284 | 292 | PF00069 | 0.425 |
DOC_PP2B_LxvP_1 | 235 | 238 | PF13499 | 0.449 |
DOC_PP2B_LxvP_1 | 403 | 406 | PF13499 | 0.425 |
DOC_PP2B_LxvP_1 | 594 | 597 | PF13499 | 0.736 |
DOC_PP4_FxxP_1 | 486 | 489 | PF00568 | 0.425 |
DOC_USP7_MATH_1 | 314 | 318 | PF00917 | 0.527 |
DOC_USP7_MATH_1 | 620 | 624 | PF00917 | 0.612 |
DOC_USP7_MATH_2 | 281 | 287 | PF00917 | 0.425 |
DOC_USP7_UBL2_3 | 27 | 31 | PF12436 | 0.673 |
DOC_USP7_UBL2_3 | 586 | 590 | PF12436 | 0.717 |
DOC_WW_Pin1_4 | 146 | 151 | PF00397 | 0.583 |
DOC_WW_Pin1_4 | 32 | 37 | PF00397 | 0.469 |
DOC_WW_Pin1_4 | 584 | 589 | PF00397 | 0.619 |
DOC_WW_Pin1_4 | 596 | 601 | PF00397 | 0.502 |
LIG_14-3-3_CanoR_1 | 144 | 150 | PF00244 | 0.536 |
LIG_14-3-3_CanoR_1 | 19 | 24 | PF00244 | 0.642 |
LIG_14-3-3_CanoR_1 | 257 | 262 | PF00244 | 0.449 |
LIG_14-3-3_CanoR_1 | 365 | 370 | PF00244 | 0.436 |
LIG_14-3-3_CanoR_1 | 430 | 438 | PF00244 | 0.452 |
LIG_14-3-3_CanoR_1 | 556 | 566 | PF00244 | 0.574 |
LIG_14-3-3_CanoR_1 | 593 | 597 | PF00244 | 0.527 |
LIG_14-3-3_CanoR_1 | 621 | 625 | PF00244 | 0.496 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.588 |
LIG_eIF4E_1 | 222 | 228 | PF01652 | 0.230 |
LIG_FHA_1 | 166 | 172 | PF00498 | 0.542 |
LIG_FHA_1 | 188 | 194 | PF00498 | 0.407 |
LIG_FHA_1 | 20 | 26 | PF00498 | 0.498 |
LIG_FHA_1 | 253 | 259 | PF00498 | 0.437 |
LIG_FHA_1 | 341 | 347 | PF00498 | 0.464 |
LIG_FHA_1 | 351 | 357 | PF00498 | 0.461 |
LIG_FHA_1 | 377 | 383 | PF00498 | 0.453 |
LIG_FHA_1 | 408 | 414 | PF00498 | 0.493 |
LIG_FHA_2 | 177 | 183 | PF00498 | 0.423 |
LIG_FHA_2 | 382 | 388 | PF00498 | 0.475 |
LIG_FHA_2 | 81 | 87 | PF00498 | 0.493 |
LIG_LIR_Gen_1 | 209 | 218 | PF02991 | 0.336 |
LIG_LIR_Gen_1 | 223 | 232 | PF02991 | 0.356 |
LIG_LIR_Gen_1 | 283 | 293 | PF02991 | 0.425 |
LIG_LIR_Gen_1 | 389 | 398 | PF02991 | 0.542 |
LIG_LIR_Gen_1 | 90 | 95 | PF02991 | 0.580 |
LIG_LIR_Nem_3 | 209 | 213 | PF02991 | 0.375 |
LIG_LIR_Nem_3 | 223 | 227 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 283 | 288 | PF02991 | 0.425 |
LIG_LIR_Nem_3 | 317 | 321 | PF02991 | 0.290 |
LIG_LIR_Nem_3 | 389 | 394 | PF02991 | 0.500 |
LIG_LIR_Nem_3 | 90 | 94 | PF02991 | 0.578 |
LIG_MAD2 | 331 | 339 | PF02301 | 0.464 |
LIG_PCNA_PIPBox_1 | 229 | 238 | PF02747 | 0.364 |
LIG_PCNA_yPIPBox_3 | 167 | 176 | PF02747 | 0.462 |
LIG_REV1ctd_RIR_1 | 517 | 527 | PF16727 | 0.436 |
LIG_SH2_NCK_1 | 425 | 429 | PF00017 | 0.392 |
LIG_SH2_SRC | 425 | 428 | PF00017 | 0.392 |
LIG_SH2_STAP1 | 391 | 395 | PF00017 | 0.436 |
LIG_SH2_STAT3 | 310 | 313 | PF00017 | 0.425 |
LIG_SH2_STAT3 | 345 | 348 | PF00017 | 0.425 |
LIG_SH2_STAT5 | 210 | 213 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 305 | 308 | PF00017 | 0.448 |
LIG_SH2_STAT5 | 345 | 348 | PF00017 | 0.425 |
LIG_SH2_STAT5 | 451 | 454 | PF00017 | 0.436 |
LIG_SH2_STAT5 | 509 | 512 | PF00017 | 0.492 |
LIG_SH3_3 | 358 | 364 | PF00018 | 0.449 |
LIG_SH3_3 | 594 | 600 | PF00018 | 0.548 |
LIG_SUMO_SIM_anti_2 | 209 | 215 | PF11976 | 0.406 |
LIG_SUMO_SIM_par_1 | 217 | 223 | PF11976 | 0.398 |
LIG_TRAF2_1 | 179 | 182 | PF00917 | 0.332 |
LIG_TRAF2_1 | 325 | 328 | PF00917 | 0.450 |
LIG_TRAF2_1 | 55 | 58 | PF00917 | 0.771 |
LIG_TRAF2_1 | 62 | 65 | PF00917 | 0.722 |
LIG_TRAF2_1 | 97 | 100 | PF00917 | 0.575 |
LIG_TYR_ITSM | 387 | 394 | PF00017 | 0.479 |
MOD_CDK_SPxK_1 | 584 | 590 | PF00069 | 0.619 |
MOD_CDK_SPxxK_3 | 596 | 603 | PF00069 | 0.617 |
MOD_CK1_1 | 368 | 374 | PF00069 | 0.362 |
MOD_CK1_1 | 455 | 461 | PF00069 | 0.464 |
MOD_CK1_1 | 528 | 534 | PF00069 | 0.540 |
MOD_CK1_1 | 549 | 555 | PF00069 | 0.714 |
MOD_CK1_1 | 584 | 590 | PF00069 | 0.615 |
MOD_CK2_1 | 176 | 182 | PF00069 | 0.430 |
MOD_CK2_1 | 386 | 392 | PF00069 | 0.527 |
MOD_CK2_1 | 80 | 86 | PF00069 | 0.702 |
MOD_CK2_1 | 94 | 100 | PF00069 | 0.521 |
MOD_GlcNHglycan | 334 | 338 | PF01048 | 0.303 |
MOD_GlcNHglycan | 407 | 410 | PF01048 | 0.294 |
MOD_GlcNHglycan | 440 | 443 | PF01048 | 0.253 |
MOD_GlcNHglycan | 548 | 551 | PF01048 | 0.712 |
MOD_GSK3_1 | 11 | 18 | PF00069 | 0.564 |
MOD_GSK3_1 | 142 | 149 | PF00069 | 0.587 |
MOD_GSK3_1 | 248 | 255 | PF00069 | 0.533 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.592 |
MOD_GSK3_1 | 407 | 414 | PF00069 | 0.427 |
MOD_GSK3_1 | 499 | 506 | PF00069 | 0.494 |
MOD_GSK3_1 | 525 | 532 | PF00069 | 0.484 |
MOD_GSK3_1 | 535 | 542 | PF00069 | 0.648 |
MOD_GSK3_1 | 544 | 551 | PF00069 | 0.521 |
MOD_GSK3_1 | 592 | 599 | PF00069 | 0.686 |
MOD_N-GLC_1 | 80 | 85 | PF02516 | 0.627 |
MOD_NEK2_1 | 174 | 179 | PF00069 | 0.624 |
MOD_NEK2_1 | 228 | 233 | PF00069 | 0.456 |
MOD_NEK2_1 | 248 | 253 | PF00069 | 0.504 |
MOD_NEK2_1 | 333 | 338 | PF00069 | 0.476 |
MOD_NEK2_1 | 350 | 355 | PF00069 | 0.360 |
MOD_NEK2_1 | 376 | 381 | PF00069 | 0.459 |
MOD_NEK2_1 | 438 | 443 | PF00069 | 0.462 |
MOD_NEK2_1 | 503 | 508 | PF00069 | 0.465 |
MOD_PIKK_1 | 429 | 435 | PF00454 | 0.469 |
MOD_PK_1 | 415 | 421 | PF00069 | 0.425 |
MOD_PKA_1 | 11 | 17 | PF00069 | 0.514 |
MOD_PKA_1 | 42 | 48 | PF00069 | 0.619 |
MOD_PKA_1 | 525 | 531 | PF00069 | 0.394 |
MOD_PKA_2 | 251 | 257 | PF00069 | 0.425 |
MOD_PKA_2 | 429 | 435 | PF00069 | 0.436 |
MOD_PKA_2 | 529 | 535 | PF00069 | 0.390 |
MOD_PKA_2 | 557 | 563 | PF00069 | 0.679 |
MOD_PKA_2 | 592 | 598 | PF00069 | 0.542 |
MOD_PKA_2 | 608 | 614 | PF00069 | 0.500 |
MOD_Plk_1 | 415 | 421 | PF00069 | 0.420 |
MOD_Plk_4 | 228 | 234 | PF00069 | 0.445 |
MOD_Plk_4 | 314 | 320 | PF00069 | 0.464 |
MOD_Plk_4 | 341 | 347 | PF00069 | 0.422 |
MOD_Plk_4 | 455 | 461 | PF00069 | 0.425 |
MOD_ProDKin_1 | 146 | 152 | PF00069 | 0.584 |
MOD_ProDKin_1 | 32 | 38 | PF00069 | 0.469 |
MOD_ProDKin_1 | 584 | 590 | PF00069 | 0.619 |
MOD_ProDKin_1 | 596 | 602 | PF00069 | 0.502 |
MOD_SUMO_for_1 | 117 | 120 | PF00179 | 0.463 |
MOD_SUMO_for_1 | 197 | 200 | PF00179 | 0.429 |
MOD_SUMO_rev_2 | 111 | 119 | PF00179 | 0.471 |
TRG_DiLeu_BaEn_1 | 209 | 214 | PF01217 | 0.380 |
TRG_DiLeu_BaEn_1 | 223 | 228 | PF01217 | 0.355 |
TRG_DiLeu_BaEn_2 | 239 | 245 | PF01217 | 0.472 |
TRG_DiLeu_BaEn_3 | 462 | 468 | PF01217 | 0.458 |
TRG_ENDOCYTIC_2 | 210 | 213 | PF00928 | 0.351 |
TRG_ENDOCYTIC_2 | 224 | 227 | PF00928 | 0.318 |
TRG_ENDOCYTIC_2 | 391 | 394 | PF00928 | 0.422 |
TRG_ENDOCYTIC_2 | 425 | 428 | PF00928 | 0.423 |
TRG_ER_diArg_1 | 122 | 125 | PF00400 | 0.469 |
TRG_ER_diArg_1 | 507 | 509 | PF00400 | 0.440 |
TRG_NLS_MonoExtC_3 | 553 | 558 | PF00514 | 0.665 |
TRG_NLS_MonoExtN_4 | 554 | 559 | PF00514 | 0.617 |
TRG_Pf-PMV_PEXEL_1 | 125 | 129 | PF00026 | 0.545 |
TRG_Pf-PMV_PEXEL_1 | 130 | 134 | PF00026 | 0.542 |
TRG_Pf-PMV_PEXEL_1 | 266 | 270 | PF00026 | 0.225 |
TRG_Pf-PMV_PEXEL_1 | 400 | 404 | PF00026 | 0.264 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P967 | Leptomonas seymouri | 77% | 100% |
A0A0S4KG56 | Bodo saltans | 65% | 100% |
A0A1X0NJV9 | Trypanosomatidae | 71% | 100% |
A0A3Q8IJ07 | Leishmania donovani | 27% | 99% |
A0A3Q8IJS8 | Leishmania donovani | 80% | 100% |
A0A422N5J0 | Trypanosoma rangeli | 70% | 100% |
A4I6B1 | Leishmania infantum | 79% | 100% |
C9ZN38 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 67% | 100% |
E9AEB6 | Leishmania major | 27% | 100% |
E9AHJ5 | Leishmania infantum | 27% | 99% |
E9B1G7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 100% |
Q08J23 | Homo sapiens | 25% | 81% |
Q1HFZ0 | Mus musculus | 25% | 83% |
Q28E61 | Xenopus tropicalis | 24% | 78% |
Q4Q6P5 | Leishmania major | 82% | 100% |
Q4V7N2 | Xenopus laevis | 26% | 90% |
V5BIK5 | Trypanosoma cruzi | 66% | 100% |