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: 11 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: Q4QB34
Term | Name | Level | Count |
---|---|---|---|
GO:0000154 | rRNA modification | 6 | 2 |
GO:0001510 | RNA methylation | 4 | 2 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 2 |
GO:0006364 | rRNA processing | 8 | 2 |
GO:0006396 | RNA processing | 6 | 2 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009451 | RNA modification | 5 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0016070 | RNA metabolic process | 5 | 2 |
GO:0016072 | rRNA metabolic process | 7 | 2 |
GO:0031167 | rRNA methylation | 5 | 2 |
GO:0032259 | methylation | 2 | 12 |
GO:0034470 | ncRNA processing | 7 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 2 |
GO:0034660 | ncRNA metabolic process | 6 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0043412 | macromolecule modification | 4 | 2 |
GO:0043414 | macromolecule methylation | 3 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 2 |
GO:0046483 | heterocycle metabolic process | 3 | 2 |
GO:0070475 | rRNA base methylation | 6 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:0090304 | nucleic acid metabolic process | 4 | 2 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 12 |
GO:0008168 | methyltransferase activity | 4 | 12 |
GO:0008170 | N-methyltransferase activity | 5 | 2 |
GO:0008173 | RNA methyltransferase activity | 4 | 2 |
GO:0008649 | rRNA methyltransferase activity | 5 | 2 |
GO:0008757 | S-adenosylmethionine-dependent methyltransferase activity | 5 | 2 |
GO:0016434 | rRNA (cytosine) methyltransferase activity | 6 | 2 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 12 |
GO:0071424 | rRNA (cytosine-N4-)-methyltransferase activity | 6 | 2 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 2 |
GO:0140102 | catalytic activity, acting on a rRNA | 4 | 2 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 462 | 466 | PF00656 | 0.446 |
CLV_NRD_NRD_1 | 135 | 137 | PF00675 | 0.465 |
CLV_NRD_NRD_1 | 292 | 294 | PF00675 | 0.241 |
CLV_NRD_NRD_1 | 323 | 325 | PF00675 | 0.250 |
CLV_NRD_NRD_1 | 473 | 475 | PF00675 | 0.471 |
CLV_NRD_NRD_1 | 76 | 78 | PF00675 | 0.585 |
CLV_NRD_NRD_1 | 8 | 10 | PF00675 | 0.391 |
CLV_NRD_NRD_1 | 88 | 90 | PF00675 | 0.635 |
CLV_PCSK_FUR_1 | 290 | 294 | PF00082 | 0.264 |
CLV_PCSK_KEX2_1 | 135 | 137 | PF00082 | 0.466 |
CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.459 |
CLV_PCSK_KEX2_1 | 292 | 294 | PF00082 | 0.242 |
CLV_PCSK_KEX2_1 | 323 | 325 | PF00082 | 0.250 |
CLV_PCSK_KEX2_1 | 473 | 475 | PF00082 | 0.487 |
CLV_PCSK_KEX2_1 | 48 | 50 | PF00082 | 0.506 |
CLV_PCSK_KEX2_1 | 8 | 10 | PF00082 | 0.447 |
CLV_PCSK_KEX2_1 | 88 | 90 | PF00082 | 0.722 |
CLV_PCSK_PC1ET2_1 | 135 | 137 | PF00082 | 0.466 |
CLV_PCSK_PC1ET2_1 | 2 | 4 | PF00082 | 0.459 |
CLV_PCSK_PC1ET2_1 | 48 | 50 | PF00082 | 0.560 |
CLV_PCSK_SKI1_1 | 204 | 208 | PF00082 | 0.250 |
CLV_PCSK_SKI1_1 | 231 | 235 | PF00082 | 0.250 |
CLV_PCSK_SKI1_1 | 24 | 28 | PF00082 | 0.392 |
CLV_PCSK_SKI1_1 | 73 | 77 | PF00082 | 0.636 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.474 |
DEG_SCF_FBW7_1 | 276 | 282 | PF00400 | 0.464 |
DOC_CKS1_1 | 276 | 281 | PF01111 | 0.464 |
DOC_CYCLIN_RxL_1 | 18 | 29 | PF00134 | 0.301 |
DOC_MAPK_FxFP_2 | 452 | 455 | PF00069 | 0.477 |
DOC_PP1_RVXF_1 | 361 | 368 | PF00149 | 0.450 |
DOC_PP2B_LxvP_1 | 101 | 104 | PF13499 | 0.567 |
DOC_PP4_FxxP_1 | 452 | 455 | PF00568 | 0.477 |
DOC_USP7_MATH_1 | 112 | 116 | PF00917 | 0.631 |
DOC_USP7_MATH_1 | 121 | 125 | PF00917 | 0.537 |
DOC_USP7_MATH_1 | 177 | 181 | PF00917 | 0.541 |
DOC_USP7_MATH_1 | 219 | 223 | PF00917 | 0.479 |
DOC_USP7_MATH_1 | 270 | 274 | PF00917 | 0.488 |
DOC_USP7_MATH_1 | 279 | 283 | PF00917 | 0.432 |
DOC_USP7_MATH_1 | 480 | 484 | PF00917 | 0.707 |
DOC_USP7_MATH_1 | 87 | 91 | PF00917 | 0.727 |
DOC_WW_Pin1_4 | 275 | 280 | PF00397 | 0.464 |
DOC_WW_Pin1_4 | 475 | 480 | PF00397 | 0.530 |
LIG_14-3-3_CanoR_1 | 138 | 143 | PF00244 | 0.388 |
LIG_14-3-3_CanoR_1 | 198 | 207 | PF00244 | 0.483 |
LIG_14-3-3_CanoR_1 | 323 | 329 | PF00244 | 0.503 |
LIG_14-3-3_CanoR_1 | 8 | 16 | PF00244 | 0.432 |
LIG_BIR_III_2 | 66 | 70 | PF00653 | 0.477 |
LIG_BRCT_BRCA1_1 | 123 | 127 | PF00533 | 0.504 |
LIG_BRCT_BRCA1_1 | 328 | 332 | PF00533 | 0.450 |
LIG_BRCT_BRCA1_1 | 443 | 447 | PF00533 | 0.419 |
LIG_BRCT_BRCA1_1 | 477 | 481 | PF00533 | 0.551 |
LIG_CaM_NSCaTE_8 | 372 | 379 | PF13499 | 0.541 |
LIG_DLG_GKlike_1 | 138 | 145 | PF00625 | 0.376 |
LIG_FHA_1 | 153 | 159 | PF00498 | 0.474 |
LIG_FHA_1 | 164 | 170 | PF00498 | 0.412 |
LIG_FHA_1 | 248 | 254 | PF00498 | 0.461 |
LIG_FHA_2 | 222 | 228 | PF00498 | 0.450 |
LIG_Integrin_isoDGR_2 | 161 | 163 | PF01839 | 0.297 |
LIG_LIR_Apic_2 | 451 | 455 | PF02991 | 0.454 |
LIG_LIR_Gen_1 | 124 | 134 | PF02991 | 0.667 |
LIG_LIR_Gen_1 | 141 | 149 | PF02991 | 0.241 |
LIG_LIR_Gen_1 | 209 | 219 | PF02991 | 0.463 |
LIG_LIR_Gen_1 | 273 | 279 | PF02991 | 0.582 |
LIG_LIR_Gen_1 | 327 | 336 | PF02991 | 0.582 |
LIG_LIR_LC3C_4 | 361 | 366 | PF02991 | 0.450 |
LIG_LIR_Nem_3 | 124 | 130 | PF02991 | 0.672 |
LIG_LIR_Nem_3 | 141 | 145 | PF02991 | 0.278 |
LIG_LIR_Nem_3 | 191 | 196 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 209 | 215 | PF02991 | 0.481 |
LIG_LIR_Nem_3 | 273 | 277 | PF02991 | 0.503 |
LIG_LIR_Nem_3 | 468 | 472 | PF02991 | 0.475 |
LIG_MYND_1 | 19 | 23 | PF01753 | 0.452 |
LIG_Pex14_2 | 149 | 153 | PF04695 | 0.541 |
LIG_SH2_CRK | 165 | 169 | PF00017 | 0.450 |
LIG_SH2_CRK | 196 | 200 | PF00017 | 0.535 |
LIG_SH2_GRB2like | 258 | 261 | PF00017 | 0.465 |
LIG_SH2_STAP1 | 165 | 169 | PF00017 | 0.450 |
LIG_SH2_STAP1 | 391 | 395 | PF00017 | 0.464 |
LIG_SH2_STAT5 | 165 | 168 | PF00017 | 0.450 |
LIG_SH2_STAT5 | 258 | 261 | PF00017 | 0.465 |
LIG_SH2_STAT5 | 422 | 425 | PF00017 | 0.487 |
LIG_SH3_3 | 13 | 19 | PF00018 | 0.434 |
LIG_Sin3_3 | 127 | 134 | PF02671 | 0.429 |
LIG_SUMO_SIM_par_1 | 354 | 361 | PF11976 | 0.447 |
LIG_TRAF2_1 | 304 | 307 | PF00917 | 0.547 |
LIG_TRAF2_1 | 371 | 374 | PF00917 | 0.465 |
LIG_TRAF2_1 | 434 | 437 | PF00917 | 0.547 |
LIG_TRAF2_1 | 50 | 53 | PF00917 | 0.455 |
LIG_TYR_ITIM | 140 | 145 | PF00017 | 0.318 |
MOD_CK1_1 | 406 | 412 | PF00069 | 0.516 |
MOD_CK2_1 | 177 | 183 | PF00069 | 0.490 |
MOD_CK2_1 | 221 | 227 | PF00069 | 0.450 |
MOD_CK2_1 | 38 | 44 | PF00069 | 0.465 |
MOD_CK2_1 | 387 | 393 | PF00069 | 0.466 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.450 |
MOD_GlcNHglycan | 109 | 112 | PF01048 | 0.715 |
MOD_GlcNHglycan | 115 | 118 | PF01048 | 0.705 |
MOD_GlcNHglycan | 124 | 127 | PF01048 | 0.407 |
MOD_GlcNHglycan | 150 | 153 | PF01048 | 0.291 |
MOD_GlcNHglycan | 179 | 182 | PF01048 | 0.352 |
MOD_GlcNHglycan | 267 | 270 | PF01048 | 0.267 |
MOD_GlcNHglycan | 443 | 446 | PF01048 | 0.390 |
MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.741 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.651 |
MOD_GSK3_1 | 148 | 155 | PF00069 | 0.497 |
MOD_GSK3_1 | 275 | 282 | PF00069 | 0.471 |
MOD_GSK3_1 | 319 | 326 | PF00069 | 0.485 |
MOD_GSK3_1 | 375 | 382 | PF00069 | 0.515 |
MOD_GSK3_1 | 414 | 421 | PF00069 | 0.373 |
MOD_GSK3_1 | 424 | 431 | PF00069 | 0.390 |
MOD_N-GLC_1 | 122 | 127 | PF02516 | 0.533 |
MOD_N-GLC_1 | 457 | 462 | PF02516 | 0.412 |
MOD_NEK2_1 | 113 | 118 | PF00069 | 0.593 |
MOD_NEK2_1 | 122 | 127 | PF00069 | 0.501 |
MOD_NEK2_1 | 145 | 150 | PF00069 | 0.465 |
MOD_NEK2_1 | 26 | 31 | PF00069 | 0.277 |
MOD_NEK2_1 | 332 | 337 | PF00069 | 0.439 |
MOD_NEK2_1 | 376 | 381 | PF00069 | 0.490 |
MOD_NEK2_1 | 424 | 429 | PF00069 | 0.423 |
MOD_NEK2_1 | 76 | 81 | PF00069 | 0.532 |
MOD_NEK2_2 | 279 | 284 | PF00069 | 0.464 |
MOD_PIKK_1 | 221 | 227 | PF00454 | 0.439 |
MOD_PIKK_1 | 316 | 322 | PF00454 | 0.464 |
MOD_PIKK_1 | 379 | 385 | PF00454 | 0.497 |
MOD_PIKK_1 | 414 | 420 | PF00454 | 0.420 |
MOD_PIKK_1 | 424 | 430 | PF00454 | 0.411 |
MOD_PKA_1 | 323 | 329 | PF00069 | 0.543 |
MOD_PKA_1 | 8 | 14 | PF00069 | 0.483 |
MOD_PKA_2 | 104 | 110 | PF00069 | 0.614 |
MOD_PKA_2 | 323 | 329 | PF00069 | 0.497 |
MOD_PKA_2 | 406 | 412 | PF00069 | 0.408 |
MOD_PKA_2 | 76 | 82 | PF00069 | 0.657 |
MOD_PKA_2 | 8 | 14 | PF00069 | 0.458 |
MOD_PKA_2 | 87 | 93 | PF00069 | 0.701 |
MOD_PKB_1 | 136 | 144 | PF00069 | 0.375 |
MOD_Plk_1 | 122 | 128 | PF00069 | 0.534 |
MOD_Plk_1 | 145 | 151 | PF00069 | 0.439 |
MOD_Plk_1 | 175 | 181 | PF00069 | 0.461 |
MOD_Plk_1 | 208 | 214 | PF00069 | 0.464 |
MOD_Plk_1 | 436 | 442 | PF00069 | 0.438 |
MOD_Plk_1 | 457 | 463 | PF00069 | 0.414 |
MOD_Plk_2-3 | 38 | 44 | PF00069 | 0.411 |
MOD_Plk_4 | 418 | 424 | PF00069 | 0.469 |
MOD_ProDKin_1 | 275 | 281 | PF00069 | 0.464 |
MOD_ProDKin_1 | 475 | 481 | PF00069 | 0.537 |
MOD_SUMO_rev_2 | 201 | 206 | PF00179 | 0.464 |
MOD_SUMO_rev_2 | 368 | 377 | PF00179 | 0.535 |
TRG_DiLeu_BaEn_1 | 230 | 235 | PF01217 | 0.450 |
TRG_ENDOCYTIC_2 | 142 | 145 | PF00928 | 0.305 |
TRG_ENDOCYTIC_2 | 165 | 168 | PF00928 | 0.450 |
TRG_ENDOCYTIC_2 | 274 | 277 | PF00928 | 0.448 |
TRG_ER_diArg_1 | 136 | 139 | PF00400 | 0.435 |
TRG_ER_diArg_1 | 289 | 292 | PF00400 | 0.452 |
TRG_ER_diArg_1 | 472 | 474 | PF00400 | 0.507 |
TRG_ER_diArg_1 | 7 | 9 | PF00400 | 0.394 |
TRG_NES_CRM1_1 | 346 | 361 | PF08389 | 0.449 |
TRG_NLS_Bipartite_1 | 59 | 81 | PF00514 | 0.610 |
TRG_NLS_MonoCore_2 | 134 | 139 | PF00514 | 0.449 |
TRG_NLS_MonoExtN_4 | 132 | 139 | PF00514 | 0.462 |
TRG_NLS_MonoExtN_4 | 74 | 81 | PF00514 | 0.585 |
TRG_Pf-PMV_PEXEL_1 | 182 | 186 | PF00026 | 0.301 |
TRG_Pf-PMV_PEXEL_1 | 287 | 291 | PF00026 | 0.297 |
TRG_Pf-PMV_PEXEL_1 | 40 | 44 | PF00026 | 0.381 |
TRG_Pf-PMV_PEXEL_1 | 49 | 53 | PF00026 | 0.381 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PB41 | Leptomonas seymouri | 72% | 98% |
A0A0S4J2S9 | Bodo saltans | 42% | 100% |
A0A1X0NY59 | Trypanosomatidae | 58% | 100% |
A0A3Q8IM97 | Leishmania donovani | 95% | 100% |
A0A3R7KU88 | Trypanosoma rangeli | 60% | 100% |
A4HCZ1 | Leishmania braziliensis | 86% | 100% |
A4I0H6 | Leishmania infantum | 96% | 100% |
C9ZVA0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 59% | 100% |
E9AWD8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
V5BEN6 | Trypanosoma cruzi | 62% | 100% |