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: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005829 | cytosol | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4QFS5
Term | Name | Level | Count |
---|---|---|---|
GO:0001510 | RNA methylation | 4 | 2 |
GO:0002128 | tRNA nucleoside ribose methylation | 6 | 2 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 8 |
GO:0006396 | RNA processing | 6 | 8 |
GO:0006399 | tRNA metabolic process | 7 | 2 |
GO:0006400 | tRNA modification | 6 | 2 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 8 |
GO:0006807 | nitrogen compound metabolic process | 2 | 8 |
GO:0008033 | tRNA processing | 8 | 2 |
GO:0008152 | metabolic process | 1 | 8 |
GO:0009451 | RNA modification | 5 | 2 |
GO:0009987 | cellular process | 1 | 8 |
GO:0016070 | RNA metabolic process | 5 | 8 |
GO:0030488 | tRNA methylation | 5 | 2 |
GO:0032259 | methylation | 2 | 2 |
GO:0034470 | ncRNA processing | 7 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 8 |
GO:0034660 | ncRNA metabolic process | 6 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 8 |
GO:0043412 | macromolecule modification | 4 | 2 |
GO:0043414 | macromolecule methylation | 3 | 2 |
GO:0044237 | cellular metabolic process | 2 | 8 |
GO:0044238 | primary metabolic process | 2 | 8 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 2 |
GO:0046483 | heterocycle metabolic process | 3 | 8 |
GO:0071704 | organic substance metabolic process | 2 | 8 |
GO:0090304 | nucleic acid metabolic process | 4 | 8 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 8 |
GO:0008168 | methyltransferase activity | 4 | 8 |
GO:0008171 | O-methyltransferase activity | 5 | 2 |
GO:0008173 | RNA methyltransferase activity | 4 | 8 |
GO:0008175 | tRNA methyltransferase activity | 5 | 2 |
GO:0008757 | S-adenosylmethionine-dependent methyltransferase activity | 5 | 2 |
GO:0016300 | tRNA (uracil) methyltransferase activity | 6 | 2 |
GO:0016427 | tRNA (cytosine) methyltransferase activity | 6 | 2 |
GO:0016740 | transferase activity | 2 | 8 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 8 |
GO:0052665 | tRNA (uracil-2'-O-)-methyltransferase activity | 7 | 2 |
GO:0052666 | tRNA (cytosine-2'-O-)-methyltransferase activity | 7 | 2 |
GO:0062105 | RNA 2'-O-methyltransferase activity | 5 | 2 |
GO:0106050 | tRNA 2'-O-methyltransferase activity | 6 | 2 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 8 |
GO:0140101 | catalytic activity, acting on a tRNA | 4 | 2 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 8 |
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003723 | RNA binding | 4 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_MEL_PAP_1 | 282 | 288 | PF00089 | 0.463 |
CLV_NRD_NRD_1 | 190 | 192 | PF00675 | 0.467 |
CLV_NRD_NRD_1 | 194 | 196 | PF00675 | 0.441 |
CLV_NRD_NRD_1 | 61 | 63 | PF00675 | 0.611 |
CLV_NRD_NRD_1 | 76 | 78 | PF00675 | 0.646 |
CLV_PCSK_FUR_1 | 74 | 78 | PF00082 | 0.541 |
CLV_PCSK_KEX2_1 | 144 | 146 | PF00082 | 0.709 |
CLV_PCSK_KEX2_1 | 190 | 192 | PF00082 | 0.467 |
CLV_PCSK_KEX2_1 | 194 | 196 | PF00082 | 0.441 |
CLV_PCSK_KEX2_1 | 76 | 78 | PF00082 | 0.531 |
CLV_PCSK_PC1ET2_1 | 144 | 146 | PF00082 | 0.709 |
CLV_PCSK_PC7_1 | 190 | 196 | PF00082 | 0.343 |
CLV_PCSK_PC7_1 | 72 | 78 | PF00082 | 0.515 |
CLV_PCSK_SKI1_1 | 190 | 194 | PF00082 | 0.491 |
CLV_PCSK_SKI1_1 | 469 | 473 | PF00082 | 0.517 |
DEG_SPOP_SBC_1 | 47 | 51 | PF00917 | 0.662 |
DOC_CKS1_1 | 221 | 226 | PF01111 | 0.392 |
DOC_CYCLIN_yCln2_LP_2 | 239 | 245 | PF00134 | 0.509 |
DOC_CYCLIN_yCln2_LP_2 | 82 | 88 | PF00134 | 0.535 |
DOC_MAPK_gen_1 | 74 | 82 | PF00069 | 0.501 |
DOC_MAPK_MEF2A_6 | 318 | 325 | PF00069 | 0.447 |
DOC_PP1_SILK_1 | 228 | 233 | PF00149 | 0.377 |
DOC_PP2B_LxvP_1 | 323 | 326 | PF13499 | 0.426 |
DOC_PP2B_LxvP_1 | 82 | 85 | PF13499 | 0.452 |
DOC_PP4_FxxP_1 | 375 | 378 | PF00568 | 0.495 |
DOC_USP7_MATH_1 | 21 | 25 | PF00917 | 0.814 |
DOC_USP7_MATH_1 | 274 | 278 | PF00917 | 0.580 |
DOC_USP7_MATH_1 | 349 | 353 | PF00917 | 0.574 |
DOC_USP7_MATH_1 | 47 | 51 | PF00917 | 0.657 |
DOC_WW_Pin1_4 | 206 | 211 | PF00397 | 0.612 |
DOC_WW_Pin1_4 | 220 | 225 | PF00397 | 0.333 |
DOC_WW_Pin1_4 | 23 | 28 | PF00397 | 0.674 |
DOC_WW_Pin1_4 | 30 | 35 | PF00397 | 0.591 |
DOC_WW_Pin1_4 | 345 | 350 | PF00397 | 0.725 |
DOC_WW_Pin1_4 | 43 | 48 | PF00397 | 0.552 |
DOC_WW_Pin1_4 | 483 | 488 | PF00397 | 0.563 |
LIG_14-3-3_CanoR_1 | 156 | 166 | PF00244 | 0.693 |
LIG_FHA_1 | 109 | 115 | PF00498 | 0.489 |
LIG_FHA_1 | 251 | 257 | PF00498 | 0.654 |
LIG_FHA_1 | 377 | 383 | PF00498 | 0.712 |
LIG_FHA_1 | 38 | 44 | PF00498 | 0.623 |
LIG_FHA_1 | 390 | 396 | PF00498 | 0.691 |
LIG_FHA_1 | 436 | 442 | PF00498 | 0.417 |
LIG_FHA_1 | 49 | 55 | PF00498 | 0.534 |
LIG_FHA_1 | 98 | 104 | PF00498 | 0.533 |
LIG_FHA_2 | 158 | 164 | PF00498 | 0.697 |
LIG_FHA_2 | 182 | 188 | PF00498 | 0.560 |
LIG_LIR_Gen_1 | 125 | 132 | PF02991 | 0.508 |
LIG_LIR_Gen_1 | 329 | 339 | PF02991 | 0.388 |
LIG_LIR_Nem_3 | 125 | 131 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 329 | 335 | PF02991 | 0.364 |
LIG_LIR_Nem_3 | 466 | 471 | PF02991 | 0.488 |
LIG_NRBOX | 188 | 194 | PF00104 | 0.408 |
LIG_Pex14_1 | 468 | 472 | PF04695 | 0.504 |
LIG_SH2_CRK | 444 | 448 | PF00017 | 0.425 |
LIG_SH2_NCK_1 | 371 | 375 | PF00017 | 0.455 |
LIG_SH2_SRC | 305 | 308 | PF00017 | 0.457 |
LIG_SH2_SRC | 371 | 374 | PF00017 | 0.451 |
LIG_SH2_STAP1 | 128 | 132 | PF00017 | 0.505 |
LIG_SH2_STAP1 | 305 | 309 | PF00017 | 0.515 |
LIG_SH2_STAT3 | 339 | 342 | PF00017 | 0.463 |
LIG_SH2_STAT5 | 403 | 406 | PF00017 | 0.371 |
LIG_SH3_3 | 215 | 221 | PF00018 | 0.405 |
LIG_SH3_3 | 343 | 349 | PF00018 | 0.598 |
LIG_SH3_3 | 379 | 385 | PF00018 | 0.501 |
LIG_SH3_3 | 422 | 428 | PF00018 | 0.369 |
LIG_SUMO_SIM_par_1 | 355 | 360 | PF11976 | 0.360 |
LIG_TRAF2_1 | 159 | 162 | PF00917 | 0.632 |
LIG_TRAF2_1 | 252 | 255 | PF00917 | 0.620 |
LIG_TYR_ITIM | 442 | 447 | PF00017 | 0.411 |
LIG_WRC_WIRS_1 | 286 | 291 | PF05994 | 0.427 |
MOD_CK1_1 | 108 | 114 | PF00069 | 0.549 |
MOD_CK1_1 | 140 | 146 | PF00069 | 0.622 |
MOD_CK1_1 | 23 | 29 | PF00069 | 0.711 |
MOD_CK1_1 | 350 | 356 | PF00069 | 0.530 |
MOD_CK1_1 | 376 | 382 | PF00069 | 0.698 |
MOD_CK1_1 | 46 | 52 | PF00069 | 0.660 |
MOD_CK1_1 | 463 | 469 | PF00069 | 0.574 |
MOD_CK2_1 | 157 | 163 | PF00069 | 0.648 |
MOD_CK2_1 | 181 | 187 | PF00069 | 0.457 |
MOD_CK2_1 | 249 | 255 | PF00069 | 0.710 |
MOD_DYRK1A_RPxSP_1 | 347 | 351 | PF00069 | 0.546 |
MOD_GlcNHglycan | 107 | 110 | PF01048 | 0.567 |
MOD_GlcNHglycan | 11 | 14 | PF01048 | 0.638 |
MOD_GlcNHglycan | 276 | 279 | PF01048 | 0.647 |
MOD_GlcNHglycan | 291 | 294 | PF01048 | 0.357 |
MOD_GlcNHglycan | 412 | 415 | PF01048 | 0.433 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.542 |
MOD_GSK3_1 | 133 | 140 | PF00069 | 0.626 |
MOD_GSK3_1 | 157 | 164 | PF00069 | 0.699 |
MOD_GSK3_1 | 245 | 252 | PF00069 | 0.647 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.635 |
MOD_GSK3_1 | 274 | 281 | PF00069 | 0.741 |
MOD_GSK3_1 | 285 | 292 | PF00069 | 0.508 |
MOD_GSK3_1 | 345 | 352 | PF00069 | 0.581 |
MOD_GSK3_1 | 43 | 50 | PF00069 | 0.653 |
MOD_N-GLC_1 | 206 | 211 | PF02516 | 0.662 |
MOD_NEK2_1 | 137 | 142 | PF00069 | 0.671 |
MOD_NEK2_1 | 259 | 264 | PF00069 | 0.607 |
MOD_NEK2_1 | 289 | 294 | PF00069 | 0.366 |
MOD_NEK2_1 | 435 | 440 | PF00069 | 0.415 |
MOD_NEK2_1 | 481 | 486 | PF00069 | 0.502 |
MOD_NEK2_2 | 122 | 127 | PF00069 | 0.492 |
MOD_NEK2_2 | 278 | 283 | PF00069 | 0.528 |
MOD_PIKK_1 | 137 | 143 | PF00454 | 0.690 |
MOD_PIKK_1 | 169 | 175 | PF00454 | 0.624 |
MOD_PIKK_1 | 376 | 382 | PF00454 | 0.698 |
MOD_PKA_2 | 157 | 163 | PF00069 | 0.698 |
MOD_PKA_2 | 169 | 175 | PF00069 | 0.549 |
MOD_PKA_2 | 445 | 451 | PF00069 | 0.359 |
MOD_PKA_2 | 481 | 487 | PF00069 | 0.591 |
MOD_PKB_1 | 283 | 291 | PF00069 | 0.453 |
MOD_Plk_1 | 133 | 139 | PF00069 | 0.559 |
MOD_Plk_1 | 161 | 167 | PF00069 | 0.636 |
MOD_Plk_4 | 161 | 167 | PF00069 | 0.697 |
MOD_Plk_4 | 285 | 291 | PF00069 | 0.430 |
MOD_ProDKin_1 | 206 | 212 | PF00069 | 0.594 |
MOD_ProDKin_1 | 220 | 226 | PF00069 | 0.329 |
MOD_ProDKin_1 | 23 | 29 | PF00069 | 0.675 |
MOD_ProDKin_1 | 30 | 36 | PF00069 | 0.591 |
MOD_ProDKin_1 | 345 | 351 | PF00069 | 0.720 |
MOD_ProDKin_1 | 43 | 49 | PF00069 | 0.554 |
TRG_DiLeu_BaEn_4 | 254 | 260 | PF01217 | 0.511 |
TRG_DiLeu_BaLyEn_6 | 188 | 193 | PF01217 | 0.456 |
TRG_DiLeu_BaLyEn_6 | 209 | 214 | PF01217 | 0.486 |
TRG_ENDOCYTIC_2 | 128 | 131 | PF00928 | 0.513 |
TRG_ENDOCYTIC_2 | 444 | 447 | PF00928 | 0.422 |
TRG_ENDOCYTIC_2 | 95 | 98 | PF00928 | 0.538 |
TRG_ER_diArg_1 | 189 | 191 | PF00400 | 0.462 |
TRG_ER_diArg_1 | 193 | 195 | PF00400 | 0.438 |
TRG_ER_diArg_1 | 282 | 285 | PF00400 | 0.504 |
TRG_ER_diArg_1 | 480 | 483 | PF00400 | 0.537 |
TRG_ER_diArg_1 | 73 | 76 | PF00400 | 0.657 |
TRG_Pf-PMV_PEXEL_1 | 130 | 134 | PF00026 | 0.553 |
TRG_Pf-PMV_PEXEL_1 | 318 | 322 | PF00026 | 0.490 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IIC5 | Leptomonas seymouri | 50% | 94% |
A0A3S7WSX9 | Leishmania donovani | 93% | 100% |
A4H7L7 | Leishmania braziliensis | 69% | 93% |
A4HW02 | Leishmania infantum | 93% | 100% |
E9APQ4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 96% |
V5BIX5 | Trypanosoma cruzi | 31% | 100% |