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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 9 |
GO:0005737 | cytoplasm | 2 | 10 |
GO:0043226 | organelle | 2 | 10 |
GO:0043227 | membrane-bounded organelle | 3 | 9 |
GO:0043229 | intracellular organelle | 3 | 10 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
GO:0005730 | nucleolus | 5 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
Related structures:
AlphaFold database: A4HAZ1
Term | Name | Level | Count |
---|---|---|---|
GO:0000154 | rRNA modification | 6 | 11 |
GO:0001510 | RNA methylation | 4 | 11 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 11 |
GO:0006364 | rRNA processing | 8 | 11 |
GO:0006396 | RNA processing | 6 | 11 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 11 |
GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0009451 | RNA modification | 5 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0016070 | RNA metabolic process | 5 | 11 |
GO:0016072 | rRNA metabolic process | 7 | 11 |
GO:0031167 | rRNA methylation | 5 | 11 |
GO:0032259 | methylation | 2 | 11 |
GO:0034470 | ncRNA processing | 7 | 11 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 11 |
GO:0034660 | ncRNA metabolic process | 6 | 11 |
GO:0036265 | RNA (guanine-N7)-methylation | 5 | 11 |
GO:0043170 | macromolecule metabolic process | 3 | 11 |
GO:0043412 | macromolecule modification | 4 | 11 |
GO:0043414 | macromolecule methylation | 3 | 11 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 11 |
GO:0046483 | heterocycle metabolic process | 3 | 11 |
GO:0070475 | rRNA base methylation | 6 | 11 |
GO:0070476 | rRNA (guanine-N7)-methylation | 6 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:0090304 | nucleic acid metabolic process | 4 | 11 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 11 |
GO:0008168 | methyltransferase activity | 4 | 11 |
GO:0008173 | RNA methyltransferase activity | 4 | 11 |
GO:0008649 | rRNA methyltransferase activity | 5 | 11 |
GO:0008757 | S-adenosylmethionine-dependent methyltransferase activity | 5 | 11 |
GO:0016435 | rRNA (guanine) methyltransferase activity | 6 | 11 |
GO:0016740 | transferase activity | 2 | 11 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 11 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 11 |
GO:0140102 | catalytic activity, acting on a rRNA | 4 | 11 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 314 | 318 | PF00656 | 0.728 |
CLV_C14_Caspase3-7 | 323 | 327 | PF00656 | 0.725 |
CLV_C14_Caspase3-7 | 410 | 414 | PF00656 | 0.527 |
CLV_NRD_NRD_1 | 22 | 24 | PF00675 | 0.547 |
CLV_NRD_NRD_1 | 229 | 231 | PF00675 | 0.419 |
CLV_NRD_NRD_1 | 243 | 245 | PF00675 | 0.428 |
CLV_NRD_NRD_1 | 31 | 33 | PF00675 | 0.510 |
CLV_NRD_NRD_1 | 353 | 355 | PF00675 | 0.724 |
CLV_NRD_NRD_1 | 382 | 384 | PF00675 | 0.285 |
CLV_NRD_NRD_1 | 405 | 407 | PF00675 | 0.287 |
CLV_NRD_NRD_1 | 420 | 422 | PF00675 | 0.306 |
CLV_PCSK_FUR_1 | 29 | 33 | PF00082 | 0.336 |
CLV_PCSK_FUR_1 | 380 | 384 | PF00082 | 0.368 |
CLV_PCSK_FUR_1 | 403 | 407 | PF00082 | 0.339 |
CLV_PCSK_KEX2_1 | 22 | 24 | PF00082 | 0.595 |
CLV_PCSK_KEX2_1 | 229 | 231 | PF00082 | 0.415 |
CLV_PCSK_KEX2_1 | 243 | 245 | PF00082 | 0.428 |
CLV_PCSK_KEX2_1 | 31 | 33 | PF00082 | 0.545 |
CLV_PCSK_KEX2_1 | 355 | 357 | PF00082 | 0.704 |
CLV_PCSK_KEX2_1 | 369 | 371 | PF00082 | 0.234 |
CLV_PCSK_KEX2_1 | 382 | 384 | PF00082 | 0.279 |
CLV_PCSK_KEX2_1 | 403 | 405 | PF00082 | 0.282 |
CLV_PCSK_PC1ET2_1 | 355 | 357 | PF00082 | 0.704 |
CLV_PCSK_PC1ET2_1 | 369 | 371 | PF00082 | 0.234 |
CLV_PCSK_PC7_1 | 378 | 384 | PF00082 | 0.325 |
CLV_PCSK_SKI1_1 | 244 | 248 | PF00082 | 0.479 |
CLV_PCSK_SKI1_1 | 35 | 39 | PF00082 | 0.404 |
CLV_PCSK_SKI1_1 | 387 | 391 | PF00082 | 0.296 |
CLV_PCSK_SKI1_1 | 96 | 100 | PF00082 | 0.439 |
DEG_Kelch_Keap1_1 | 327 | 332 | PF01344 | 0.530 |
DOC_MAPK_gen_1 | 285 | 293 | PF00069 | 0.403 |
DOC_MAPK_gen_1 | 29 | 39 | PF00069 | 0.509 |
DOC_PP2B_LxvP_1 | 45 | 48 | PF13499 | 0.492 |
DOC_PP4_FxxP_1 | 302 | 305 | PF00568 | 0.506 |
DOC_USP7_MATH_1 | 175 | 179 | PF00917 | 0.729 |
DOC_USP7_MATH_1 | 371 | 375 | PF00917 | 0.547 |
LIG_14-3-3_CanoR_1 | 22 | 27 | PF00244 | 0.460 |
LIG_14-3-3_CanoR_1 | 406 | 416 | PF00244 | 0.562 |
LIG_Actin_WH2_2 | 227 | 245 | PF00022 | 0.443 |
LIG_Actin_WH2_2 | 81 | 98 | PF00022 | 0.526 |
LIG_EVH1_2 | 11 | 15 | PF00568 | 0.542 |
LIG_FHA_1 | 130 | 136 | PF00498 | 0.636 |
LIG_FHA_1 | 307 | 313 | PF00498 | 0.614 |
LIG_FHA_2 | 408 | 414 | PF00498 | 0.482 |
LIG_LIR_Gen_1 | 237 | 246 | PF02991 | 0.433 |
LIG_LIR_Gen_1 | 392 | 402 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 237 | 242 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 392 | 398 | PF02991 | 0.482 |
LIG_PCNA_PIPBox_1 | 228 | 237 | PF02747 | 0.404 |
LIG_PCNA_yPIPBox_3 | 222 | 235 | PF02747 | 0.427 |
LIG_SH2_CRK | 239 | 243 | PF00017 | 0.383 |
LIG_SH2_STAT5 | 24 | 27 | PF00017 | 0.431 |
LIG_SH2_STAT5 | 290 | 293 | PF00017 | 0.375 |
LIG_SH2_STAT5 | 416 | 419 | PF00017 | 0.482 |
LIG_SH3_3 | 196 | 202 | PF00018 | 0.414 |
LIG_SH3_3 | 251 | 257 | PF00018 | 0.527 |
LIG_SH3_3 | 275 | 281 | PF00018 | 0.416 |
LIG_SH3_3 | 300 | 306 | PF00018 | 0.440 |
LIG_SUMO_SIM_anti_2 | 210 | 215 | PF11976 | 0.473 |
LIG_SUMO_SIM_par_1 | 63 | 69 | PF11976 | 0.531 |
LIG_UBA3_1 | 44 | 49 | PF00899 | 0.566 |
LIG_UBA3_1 | 94 | 99 | PF00899 | 0.406 |
MOD_CK1_1 | 327 | 333 | PF00069 | 0.741 |
MOD_CK1_1 | 414 | 420 | PF00069 | 0.478 |
MOD_CK1_1 | 71 | 77 | PF00069 | 0.407 |
MOD_CK2_1 | 252 | 258 | PF00069 | 0.501 |
MOD_CK2_1 | 326 | 332 | PF00069 | 0.644 |
MOD_GlcNHglycan | 151 | 154 | PF01048 | 0.734 |
MOD_GlcNHglycan | 166 | 169 | PF01048 | 0.818 |
MOD_GlcNHglycan | 172 | 175 | PF01048 | 0.809 |
MOD_GlcNHglycan | 177 | 180 | PF01048 | 0.752 |
MOD_GlcNHglycan | 282 | 285 | PF01048 | 0.485 |
MOD_GlcNHglycan | 326 | 329 | PF01048 | 0.662 |
MOD_GlcNHglycan | 336 | 339 | PF01048 | 0.760 |
MOD_GlcNHglycan | 374 | 377 | PF01048 | 0.311 |
MOD_GlcNHglycan | 60 | 63 | PF01048 | 0.510 |
MOD_GlcNHglycan | 68 | 71 | PF01048 | 0.449 |
MOD_GlcNHglycan | 73 | 76 | PF01048 | 0.351 |
MOD_GSK3_1 | 164 | 171 | PF00069 | 0.782 |
MOD_GSK3_1 | 311 | 318 | PF00069 | 0.752 |
MOD_GSK3_1 | 320 | 327 | PF00069 | 0.753 |
MOD_GSK3_1 | 407 | 414 | PF00069 | 0.482 |
MOD_N-GLC_1 | 16 | 21 | PF02516 | 0.465 |
MOD_N-GLC_1 | 58 | 63 | PF02516 | 0.601 |
MOD_NEK2_1 | 121 | 126 | PF00069 | 0.681 |
MOD_NEK2_1 | 130 | 135 | PF00069 | 0.674 |
MOD_NEK2_1 | 217 | 222 | PF00069 | 0.501 |
MOD_NEK2_1 | 234 | 239 | PF00069 | 0.295 |
MOD_NEK2_1 | 334 | 339 | PF00069 | 0.497 |
MOD_NEK2_1 | 348 | 353 | PF00069 | 0.469 |
MOD_PKA_1 | 22 | 28 | PF00069 | 0.554 |
MOD_PKA_2 | 169 | 175 | PF00069 | 0.552 |
MOD_PKA_2 | 22 | 28 | PF00069 | 0.462 |
MOD_PKA_2 | 371 | 377 | PF00069 | 0.554 |
MOD_PKB_1 | 370 | 378 | PF00069 | 0.538 |
MOD_Plk_1 | 130 | 136 | PF00069 | 0.705 |
MOD_Plk_1 | 35 | 41 | PF00069 | 0.499 |
MOD_Plk_1 | 58 | 64 | PF00069 | 0.561 |
MOD_Plk_2-3 | 311 | 317 | PF00069 | 0.657 |
MOD_Plk_2-3 | 320 | 326 | PF00069 | 0.689 |
MOD_Plk_4 | 234 | 240 | PF00069 | 0.422 |
MOD_SUMO_for_1 | 398 | 401 | PF00179 | 0.534 |
TRG_DiLeu_BaEn_1 | 258 | 263 | PF01217 | 0.315 |
TRG_ENDOCYTIC_2 | 105 | 108 | PF00928 | 0.655 |
TRG_ENDOCYTIC_2 | 239 | 242 | PF00928 | 0.376 |
TRG_ENDOCYTIC_2 | 289 | 292 | PF00928 | 0.387 |
TRG_ER_diArg_1 | 22 | 24 | PF00400 | 0.584 |
TRG_ER_diArg_1 | 229 | 231 | PF00400 | 0.412 |
TRG_ER_diArg_1 | 242 | 244 | PF00400 | 0.406 |
TRG_ER_diArg_1 | 29 | 32 | PF00400 | 0.477 |
TRG_ER_diArg_1 | 354 | 357 | PF00400 | 0.682 |
TRG_ER_diArg_1 | 380 | 383 | PF00400 | 0.510 |
TRG_ER_diArg_1 | 403 | 406 | PF00400 | 0.534 |
TRG_ER_diArg_1 | 418 | 421 | PF00400 | 0.412 |
TRG_NLS_Bipartite_1 | 354 | 373 | PF00514 | 0.397 |
TRG_NLS_Bipartite_1 | 403 | 425 | PF00514 | 0.496 |
TRG_NLS_MonoCore_2 | 420 | 425 | PF00514 | 0.678 |
TRG_NLS_MonoExtC_3 | 353 | 358 | PF00514 | 0.786 |
TRG_NLS_MonoExtN_4 | 354 | 359 | PF00514 | 0.735 |
TRG_NLS_MonoExtN_4 | 419 | 425 | PF00514 | 0.496 |
TRG_PTS1 | 422 | 425 | PF00515 | 0.586 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PC68 | Leptomonas seymouri | 71% | 100% |
A0A1X0P9R3 | Trypanosomatidae | 52% | 100% |
A0A3Q8IFP3 | Leishmania donovani | 80% | 100% |
A0A3R7KRG3 | Trypanosoma rangeli | 52% | 100% |
A4IA51 | Leishmania infantum | 80% | 100% |
C9ZM51 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 48% | 100% |
E9B565 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |
Q4Q2S0 | Leishmania major | 83% | 100% |
V5B593 | Trypanosoma cruzi | 52% | 100% |