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: A4HCZ1
Term | Name | Level | Count |
---|---|---|---|
GO:0008152 | metabolic process | 1 | 12 |
GO:0032259 | methylation | 2 | 12 |
GO:0000154 | rRNA modification | 6 | 1 |
GO:0001510 | RNA methylation | 4 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006364 | rRNA processing | 8 | 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:0009451 | RNA modification | 5 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0016072 | rRNA metabolic process | 7 | 1 |
GO:0031167 | rRNA methylation | 5 | 1 |
GO:0034470 | ncRNA processing | 7 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0034660 | ncRNA metabolic process | 6 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0043414 | macromolecule methylation | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0070475 | rRNA base methylation | 6 | 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 | 12 |
GO:0008168 | methyltransferase activity | 4 | 12 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 12 |
GO:0008170 | N-methyltransferase activity | 5 | 1 |
GO:0008173 | RNA methyltransferase activity | 4 | 1 |
GO:0008649 | rRNA methyltransferase activity | 5 | 1 |
GO:0008757 | S-adenosylmethionine-dependent methyltransferase activity | 5 | 1 |
GO:0016434 | rRNA (cytosine) methyltransferase activity | 6 | 1 |
GO:0071424 | rRNA (cytosine-N4-)-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 | 127 | 131 | PF00656 | 0.441 |
CLV_NRD_NRD_1 | 183 | 185 | PF00675 | 0.174 |
CLV_NRD_NRD_1 | 294 | 296 | PF00675 | 0.252 |
CLV_NRD_NRD_1 | 325 | 327 | PF00675 | 0.261 |
CLV_NRD_NRD_1 | 467 | 469 | PF00675 | 0.482 |
CLV_NRD_NRD_1 | 475 | 477 | PF00675 | 0.499 |
CLV_NRD_NRD_1 | 62 | 64 | PF00675 | 0.461 |
CLV_NRD_NRD_1 | 77 | 79 | PF00675 | 0.641 |
CLV_NRD_NRD_1 | 89 | 91 | PF00675 | 0.653 |
CLV_NRD_NRD_1 | 96 | 98 | PF00675 | 0.727 |
CLV_PCSK_FUR_1 | 292 | 296 | PF00082 | 0.275 |
CLV_PCSK_KEX2_1 | 139 | 141 | PF00082 | 0.489 |
CLV_PCSK_KEX2_1 | 193 | 195 | PF00082 | 0.174 |
CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.479 |
CLV_PCSK_KEX2_1 | 294 | 296 | PF00082 | 0.253 |
CLV_PCSK_KEX2_1 | 325 | 327 | PF00082 | 0.261 |
CLV_PCSK_KEX2_1 | 475 | 477 | PF00082 | 0.513 |
CLV_PCSK_KEX2_1 | 48 | 50 | PF00082 | 0.534 |
CLV_PCSK_KEX2_1 | 62 | 64 | PF00082 | 0.424 |
CLV_PCSK_KEX2_1 | 8 | 10 | PF00082 | 0.474 |
CLV_PCSK_KEX2_1 | 89 | 91 | PF00082 | 0.723 |
CLV_PCSK_KEX2_1 | 96 | 98 | PF00082 | 0.747 |
CLV_PCSK_PC1ET2_1 | 139 | 141 | PF00082 | 0.489 |
CLV_PCSK_PC1ET2_1 | 193 | 195 | PF00082 | 0.174 |
CLV_PCSK_PC1ET2_1 | 2 | 4 | PF00082 | 0.479 |
CLV_PCSK_PC1ET2_1 | 48 | 50 | PF00082 | 0.558 |
CLV_PCSK_PC1ET2_1 | 8 | 10 | PF00082 | 0.474 |
CLV_PCSK_PC7_1 | 135 | 141 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 140 | 144 | PF00082 | 0.345 |
CLV_PCSK_SKI1_1 | 206 | 210 | PF00082 | 0.258 |
CLV_PCSK_SKI1_1 | 233 | 237 | PF00082 | 0.257 |
CLV_PCSK_SKI1_1 | 24 | 28 | PF00082 | 0.423 |
CLV_PCSK_SKI1_1 | 62 | 66 | PF00082 | 0.439 |
CLV_Separin_Metazoa | 103 | 107 | PF03568 | 0.506 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.496 |
DEG_SCF_FBW7_1 | 278 | 284 | PF00400 | 0.475 |
DEG_SPOP_SBC_1 | 115 | 119 | PF00917 | 0.510 |
DOC_CKS1_1 | 278 | 283 | PF01111 | 0.475 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 37 | 46 | PF00134 | 0.448 |
DOC_MAPK_FxFP_2 | 454 | 457 | PF00069 | 0.559 |
DOC_PP1_RVXF_1 | 363 | 370 | PF00149 | 0.461 |
DOC_PP2B_LxvP_1 | 102 | 105 | PF13499 | 0.610 |
DOC_PP4_FxxP_1 | 454 | 457 | PF00568 | 0.559 |
DOC_USP7_MATH_1 | 113 | 117 | PF00917 | 0.657 |
DOC_USP7_MATH_1 | 179 | 183 | PF00917 | 0.536 |
DOC_USP7_MATH_1 | 221 | 225 | PF00917 | 0.476 |
DOC_USP7_MATH_1 | 272 | 276 | PF00917 | 0.519 |
DOC_USP7_MATH_1 | 281 | 285 | PF00917 | 0.386 |
DOC_USP7_MATH_1 | 482 | 486 | PF00917 | 0.703 |
DOC_USP7_MATH_1 | 77 | 81 | PF00917 | 0.623 |
DOC_WW_Pin1_4 | 277 | 282 | PF00397 | 0.463 |
LIG_14-3-3_CanoR_1 | 140 | 145 | PF00244 | 0.434 |
LIG_14-3-3_CanoR_1 | 200 | 209 | PF00244 | 0.492 |
LIG_14-3-3_CanoR_1 | 325 | 331 | PF00244 | 0.508 |
LIG_14-3-3_CanoR_1 | 418 | 426 | PF00244 | 0.378 |
LIG_14-3-3_CanoR_1 | 96 | 104 | PF00244 | 0.728 |
LIG_BRCT_BRCA1_1 | 330 | 334 | PF00533 | 0.461 |
LIG_CaM_NSCaTE_8 | 374 | 381 | PF13499 | 0.536 |
LIG_FHA_1 | 141 | 147 | PF00498 | 0.453 |
LIG_FHA_1 | 155 | 161 | PF00498 | 0.484 |
LIG_FHA_1 | 166 | 172 | PF00498 | 0.419 |
LIG_FHA_2 | 224 | 230 | PF00498 | 0.459 |
LIG_Integrin_isoDGR_2 | 163 | 165 | PF01839 | 0.355 |
LIG_LIR_Apic_2 | 453 | 457 | PF02991 | 0.467 |
LIG_LIR_Gen_1 | 143 | 151 | PF02991 | 0.262 |
LIG_LIR_Gen_1 | 211 | 221 | PF02991 | 0.450 |
LIG_LIR_Gen_1 | 224 | 231 | PF02991 | 0.450 |
LIG_LIR_Gen_1 | 275 | 281 | PF02991 | 0.536 |
LIG_LIR_Gen_1 | 329 | 338 | PF02991 | 0.563 |
LIG_LIR_Gen_1 | 392 | 399 | PF02991 | 0.480 |
LIG_LIR_LC3C_4 | 363 | 368 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 143 | 147 | PF02991 | 0.304 |
LIG_LIR_Nem_3 | 211 | 217 | PF02991 | 0.434 |
LIG_LIR_Nem_3 | 224 | 228 | PF02991 | 0.450 |
LIG_LIR_Nem_3 | 275 | 279 | PF02991 | 0.503 |
LIG_LIR_Nem_3 | 329 | 335 | PF02991 | 0.388 |
LIG_LIR_Nem_3 | 392 | 396 | PF02991 | 0.480 |
LIG_LIR_Nem_3 | 470 | 474 | PF02991 | 0.491 |
LIG_MYND_1 | 19 | 23 | PF01753 | 0.545 |
LIG_Pex14_2 | 151 | 155 | PF04695 | 0.536 |
LIG_SH2_CRK | 167 | 171 | PF00017 | 0.461 |
LIG_SH2_CRK | 198 | 202 | PF00017 | 0.532 |
LIG_SH2_GRB2like | 260 | 263 | PF00017 | 0.450 |
LIG_SH2_STAP1 | 167 | 171 | PF00017 | 0.461 |
LIG_SH2_STAP1 | 393 | 397 | PF00017 | 0.475 |
LIG_SH2_STAT5 | 167 | 170 | PF00017 | 0.461 |
LIG_SH2_STAT5 | 260 | 263 | PF00017 | 0.450 |
LIG_SH2_STAT5 | 424 | 427 | PF00017 | 0.470 |
LIG_SH3_2 | 69 | 74 | PF14604 | 0.470 |
LIG_SH3_3 | 13 | 19 | PF00018 | 0.461 |
LIG_SH3_3 | 64 | 70 | PF00018 | 0.515 |
LIG_SUMO_SIM_par_1 | 302 | 309 | PF11976 | 0.471 |
LIG_TRAF2_1 | 436 | 439 | PF00917 | 0.566 |
LIG_TYR_ITIM | 142 | 147 | PF00017 | 0.349 |
LIG_TYR_ITIM | 391 | 396 | PF00017 | 0.374 |
LIG_WW_3 | 103 | 107 | PF00397 | 0.506 |
MOD_CK1_1 | 116 | 122 | PF00069 | 0.577 |
MOD_CK1_1 | 124 | 130 | PF00069 | 0.534 |
MOD_CK1_1 | 321 | 327 | PF00069 | 0.422 |
MOD_CK1_1 | 408 | 414 | PF00069 | 0.508 |
MOD_CK2_1 | 223 | 229 | PF00069 | 0.450 |
MOD_CK2_1 | 389 | 395 | PF00069 | 0.477 |
MOD_GlcNHglycan | 152 | 155 | PF01048 | 0.298 |
MOD_GlcNHglycan | 181 | 184 | PF01048 | 0.343 |
MOD_GlcNHglycan | 269 | 272 | PF01048 | 0.277 |
MOD_GlcNHglycan | 379 | 382 | PF01048 | 0.174 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.679 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.548 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.555 |
MOD_GSK3_1 | 277 | 284 | PF00069 | 0.498 |
MOD_GSK3_1 | 321 | 328 | PF00069 | 0.494 |
MOD_GSK3_1 | 377 | 384 | PF00069 | 0.518 |
MOD_GSK3_1 | 414 | 421 | PF00069 | 0.388 |
MOD_GSK3_1 | 426 | 433 | PF00069 | 0.391 |
MOD_N-GLC_1 | 459 | 464 | PF02516 | 0.418 |
MOD_NEK2_1 | 114 | 119 | PF00069 | 0.621 |
MOD_NEK2_1 | 121 | 126 | PF00069 | 0.527 |
MOD_NEK2_1 | 147 | 152 | PF00069 | 0.475 |
MOD_NEK2_1 | 334 | 339 | PF00069 | 0.450 |
MOD_NEK2_2 | 281 | 286 | PF00069 | 0.475 |
MOD_PIKK_1 | 223 | 229 | PF00454 | 0.449 |
MOD_PIKK_1 | 318 | 324 | PF00454 | 0.475 |
MOD_PIKK_1 | 381 | 387 | PF00454 | 0.555 |
MOD_PIKK_1 | 426 | 432 | PF00454 | 0.454 |
MOD_PK_1 | 8 | 14 | PF00069 | 0.345 |
MOD_PKA_1 | 325 | 331 | PF00069 | 0.537 |
MOD_PKA_1 | 8 | 14 | PF00069 | 0.508 |
MOD_PKA_2 | 105 | 111 | PF00069 | 0.690 |
MOD_PKA_2 | 325 | 331 | PF00069 | 0.555 |
MOD_PKA_2 | 408 | 414 | PF00069 | 0.412 |
MOD_PKA_2 | 77 | 83 | PF00069 | 0.691 |
MOD_PKA_2 | 8 | 14 | PF00069 | 0.476 |
MOD_PKA_2 | 95 | 101 | PF00069 | 0.755 |
MOD_Plk_1 | 147 | 153 | PF00069 | 0.450 |
MOD_Plk_1 | 210 | 216 | PF00069 | 0.475 |
MOD_Plk_1 | 438 | 444 | PF00069 | 0.454 |
MOD_Plk_1 | 459 | 465 | PF00069 | 0.418 |
MOD_Plk_4 | 124 | 130 | PF00069 | 0.403 |
MOD_Plk_4 | 420 | 426 | PF00069 | 0.477 |
MOD_ProDKin_1 | 277 | 283 | PF00069 | 0.463 |
MOD_SUMO_rev_2 | 203 | 208 | PF00179 | 0.475 |
MOD_SUMO_rev_2 | 370 | 379 | PF00179 | 0.532 |
TRG_DiLeu_BaEn_1 | 232 | 237 | PF01217 | 0.461 |
TRG_DiLeu_BaLyEn_6 | 368 | 373 | PF01217 | 0.506 |
TRG_ENDOCYTIC_2 | 144 | 147 | PF00928 | 0.337 |
TRG_ENDOCYTIC_2 | 167 | 170 | PF00928 | 0.461 |
TRG_ENDOCYTIC_2 | 249 | 252 | PF00928 | 0.513 |
TRG_ENDOCYTIC_2 | 276 | 279 | PF00928 | 0.450 |
TRG_ENDOCYTIC_2 | 393 | 396 | PF00928 | 0.487 |
TRG_ER_diArg_1 | 291 | 294 | PF00400 | 0.463 |
TRG_ER_diArg_1 | 474 | 476 | PF00400 | 0.529 |
TRG_ER_diArg_1 | 89 | 91 | PF00400 | 0.706 |
TRG_ER_diArg_1 | 95 | 97 | PF00400 | 0.708 |
TRG_NES_CRM1_1 | 347 | 363 | PF08389 | 0.462 |
TRG_NLS_Bipartite_1 | 48 | 63 | PF00514 | 0.564 |
TRG_NLS_MonoExtC_3 | 58 | 63 | PF00514 | 0.365 |
TRG_NLS_MonoExtN_4 | 56 | 63 | PF00514 | 0.530 |
TRG_NLS_MonoExtN_4 | 75 | 82 | PF00514 | 0.633 |
TRG_Pf-PMV_PEXEL_1 | 184 | 188 | PF00026 | 0.306 |
TRG_Pf-PMV_PEXEL_1 | 289 | 293 | PF00026 | 0.355 |
TRG_Pf-PMV_PEXEL_1 | 371 | 375 | PF00026 | 0.174 |
TRG_Pf-PMV_PEXEL_1 | 40 | 44 | PF00026 | 0.425 |
TRG_Pf-PMV_PEXEL_1 | 49 | 53 | PF00026 | 0.432 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PB41 | Leptomonas seymouri | 73% | 99% |
A0A0S4J2S9 | Bodo saltans | 42% | 100% |
A0A1X0NY59 | Trypanosomatidae | 58% | 100% |
A0A3Q8IM97 | Leishmania donovani | 85% | 100% |
A0A3R7KU88 | Trypanosoma rangeli | 60% | 100% |
A4I0H6 | Leishmania infantum | 86% | 100% |
B9JY62 | Agrobacterium vitis (strain S4 / ATCC BAA-846) | 26% | 100% |
C9ZVA0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 58% | 100% |
E9AWD8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
Q4QB34 | Leishmania major | 86% | 100% |
V5BEN6 | Trypanosoma cruzi | 61% | 100% |