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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005829 | cytosol | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4H7L7
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 7 |
GO:0006396 | RNA processing | 6 | 7 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 7 |
GO:0006807 | nitrogen compound metabolic process | 2 | 7 |
GO:0008152 | metabolic process | 1 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0016070 | RNA metabolic process | 5 | 7 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 7 |
GO:0043170 | macromolecule metabolic process | 3 | 7 |
GO:0044237 | cellular metabolic process | 2 | 7 |
GO:0044238 | primary metabolic process | 2 | 7 |
GO:0046483 | heterocycle metabolic process | 3 | 7 |
GO:0071704 | organic substance metabolic process | 2 | 7 |
GO:0090304 | nucleic acid metabolic process | 4 | 7 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 7 |
GO:0001510 | RNA methylation | 4 | 1 |
GO:0002128 | tRNA nucleoside ribose methylation | 6 | 1 |
GO:0006399 | tRNA metabolic process | 7 | 1 |
GO:0006400 | tRNA modification | 6 | 1 |
GO:0008033 | tRNA processing | 8 | 1 |
GO:0009451 | RNA modification | 5 | 1 |
GO:0030488 | tRNA methylation | 5 | 1 |
GO:0032259 | methylation | 2 | 1 |
GO:0034470 | ncRNA processing | 7 | 1 |
GO:0034660 | ncRNA metabolic process | 6 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0043414 | macromolecule methylation | 3 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 7 |
GO:0008168 | methyltransferase activity | 4 | 7 |
GO:0008173 | RNA methyltransferase activity | 4 | 7 |
GO:0016740 | transferase activity | 2 | 7 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 7 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 7 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 7 |
GO:0008171 | O-methyltransferase activity | 5 | 1 |
GO:0008175 | tRNA methyltransferase activity | 5 | 1 |
GO:0008757 | S-adenosylmethionine-dependent methyltransferase activity | 5 | 1 |
GO:0016300 | tRNA (uracil) methyltransferase activity | 6 | 1 |
GO:0016427 | tRNA (cytosine) methyltransferase activity | 6 | 1 |
GO:0052665 | tRNA (uracil-2'-O-)-methyltransferase activity | 7 | 1 |
GO:0052666 | tRNA (cytosine-2'-O-)-methyltransferase activity | 7 | 1 |
GO:0062105 | RNA 2'-O-methyltransferase activity | 5 | 1 |
GO:0106050 | tRNA 2'-O-methyltransferase activity | 6 | 1 |
GO:0140101 | catalytic activity, acting on a tRNA | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_MEL_PAP_1 | 313 | 319 | PF00089 | 0.409 |
CLV_NRD_NRD_1 | 206 | 208 | PF00675 | 0.484 |
CLV_NRD_NRD_1 | 490 | 492 | PF00675 | 0.416 |
CLV_NRD_NRD_1 | 80 | 82 | PF00675 | 0.532 |
CLV_NRD_NRD_1 | 95 | 97 | PF00675 | 0.504 |
CLV_PCSK_FUR_1 | 93 | 97 | PF00082 | 0.492 |
CLV_PCSK_KEX2_1 | 164 | 166 | PF00082 | 0.726 |
CLV_PCSK_KEX2_1 | 206 | 208 | PF00082 | 0.523 |
CLV_PCSK_KEX2_1 | 490 | 492 | PF00082 | 0.416 |
CLV_PCSK_KEX2_1 | 82 | 84 | PF00082 | 0.537 |
CLV_PCSK_KEX2_1 | 95 | 97 | PF00082 | 0.412 |
CLV_PCSK_PC1ET2_1 | 164 | 166 | PF00082 | 0.726 |
CLV_PCSK_PC1ET2_1 | 82 | 84 | PF00082 | 0.425 |
CLV_PCSK_PC7_1 | 91 | 97 | PF00082 | 0.415 |
CLV_PCSK_SKI1_1 | 206 | 210 | PF00082 | 0.480 |
CLV_PCSK_SKI1_1 | 484 | 488 | PF00082 | 0.285 |
CLV_PCSK_SKI1_1 | 507 | 511 | PF00082 | 0.466 |
DEG_SPOP_SBC_1 | 66 | 70 | PF00917 | 0.642 |
DOC_CKS1_1 | 237 | 242 | PF01111 | 0.410 |
DOC_CYCLIN_yCln2_LP_2 | 101 | 107 | PF00134 | 0.455 |
DOC_CYCLIN_yCln2_LP_2 | 255 | 261 | PF00134 | 0.497 |
DOC_MAPK_gen_1 | 79 | 88 | PF00069 | 0.466 |
DOC_MAPK_gen_1 | 93 | 101 | PF00069 | 0.463 |
DOC_MAPK_MEF2A_6 | 349 | 356 | PF00069 | 0.424 |
DOC_PP1_RVXF_1 | 516 | 522 | PF00149 | 0.373 |
DOC_PP1_SILK_1 | 244 | 249 | PF00149 | 0.395 |
DOC_PP2B_LxvP_1 | 101 | 104 | PF13499 | 0.430 |
DOC_PP2B_LxvP_1 | 354 | 357 | PF13499 | 0.425 |
DOC_USP7_MATH_1 | 380 | 384 | PF00917 | 0.594 |
DOC_USP7_MATH_1 | 40 | 44 | PF00917 | 0.792 |
DOC_USP7_MATH_1 | 66 | 70 | PF00917 | 0.659 |
DOC_WW_Pin1_4 | 155 | 160 | PF00397 | 0.582 |
DOC_WW_Pin1_4 | 222 | 227 | PF00397 | 0.602 |
DOC_WW_Pin1_4 | 236 | 241 | PF00397 | 0.331 |
DOC_WW_Pin1_4 | 299 | 304 | PF00397 | 0.531 |
DOC_WW_Pin1_4 | 378 | 383 | PF00397 | 0.679 |
DOC_WW_Pin1_4 | 43 | 48 | PF00397 | 0.670 |
DOC_WW_Pin1_4 | 62 | 67 | PF00397 | 0.713 |
LIG_14-3-3_CanoR_1 | 174 | 182 | PF00244 | 0.679 |
LIG_14-3-3_CanoR_1 | 264 | 268 | PF00244 | 0.488 |
LIG_14-3-3_CanoR_1 | 299 | 303 | PF00244 | 0.530 |
LIG_14-3-3_CanoR_1 | 520 | 526 | PF00244 | 0.419 |
LIG_BRCT_BRCA1_1 | 13 | 17 | PF00533 | 0.348 |
LIG_BRCT_BRCA1_1 | 318 | 322 | PF00533 | 0.283 |
LIG_FHA_1 | 117 | 123 | PF00498 | 0.606 |
LIG_FHA_1 | 128 | 134 | PF00498 | 0.392 |
LIG_FHA_1 | 268 | 274 | PF00498 | 0.679 |
LIG_FHA_1 | 282 | 288 | PF00498 | 0.572 |
LIG_FHA_1 | 300 | 306 | PF00498 | 0.476 |
LIG_FHA_1 | 356 | 362 | PF00498 | 0.284 |
LIG_FHA_1 | 474 | 480 | PF00498 | 0.363 |
LIG_FHA_1 | 520 | 526 | PF00498 | 0.516 |
LIG_FHA_2 | 174 | 180 | PF00498 | 0.698 |
LIG_FHA_2 | 280 | 286 | PF00498 | 0.527 |
LIG_FHA_2 | 299 | 305 | PF00498 | 0.767 |
LIG_FHA_2 | 408 | 414 | PF00498 | 0.475 |
LIG_Integrin_RGD_1 | 367 | 369 | PF01839 | 0.343 |
LIG_LIR_Gen_1 | 16 | 25 | PF02991 | 0.423 |
LIG_LIR_Gen_1 | 360 | 370 | PF02991 | 0.389 |
LIG_LIR_Nem_3 | 16 | 21 | PF02991 | 0.359 |
LIG_LIR_Nem_3 | 360 | 366 | PF02991 | 0.365 |
LIG_LIR_Nem_3 | 403 | 409 | PF02991 | 0.368 |
LIG_NRBOX | 204 | 210 | PF00104 | 0.401 |
LIG_Pex14_1 | 13 | 17 | PF04695 | 0.332 |
LIG_Pex14_1 | 506 | 510 | PF04695 | 0.451 |
LIG_Rb_pABgroove_1 | 357 | 365 | PF01858 | 0.342 |
LIG_SH2_CRK | 482 | 486 | PF00017 | 0.374 |
LIG_SH2_NCK_1 | 147 | 151 | PF00017 | 0.470 |
LIG_SH2_NCK_1 | 402 | 406 | PF00017 | 0.480 |
LIG_SH2_SRC | 402 | 405 | PF00017 | 0.476 |
LIG_SH2_STAP1 | 336 | 340 | PF00017 | 0.558 |
LIG_SH2_STAP1 | 482 | 486 | PF00017 | 0.292 |
LIG_SH2_STAT5 | 441 | 444 | PF00017 | 0.340 |
LIG_SH3_2 | 159 | 164 | PF14604 | 0.560 |
LIG_SH3_3 | 156 | 162 | PF00018 | 0.603 |
LIG_SH3_3 | 231 | 237 | PF00018 | 0.374 |
LIG_SH3_3 | 270 | 276 | PF00018 | 0.547 |
LIG_SH3_3 | 374 | 380 | PF00018 | 0.623 |
LIG_SH3_3 | 394 | 400 | PF00018 | 0.291 |
LIG_SH3_3 | 460 | 466 | PF00018 | 0.378 |
LIG_SH3_3 | 97 | 103 | PF00018 | 0.443 |
LIG_SUMO_SIM_anti_2 | 358 | 364 | PF11976 | 0.289 |
LIG_SUMO_SIM_anti_2 | 383 | 389 | PF11976 | 0.315 |
LIG_SUMO_SIM_par_1 | 269 | 274 | PF11976 | 0.507 |
LIG_SUMO_SIM_par_1 | 386 | 391 | PF11976 | 0.363 |
LIG_TRAF2_1 | 151 | 154 | PF00917 | 0.527 |
LIG_TRAF2_1 | 283 | 286 | PF00917 | 0.592 |
LIG_TRAF2_1 | 410 | 413 | PF00917 | 0.489 |
LIG_TYR_ITIM | 480 | 485 | PF00017 | 0.360 |
LIG_WRC_WIRS_1 | 317 | 322 | PF05994 | 0.441 |
MOD_CK1_1 | 127 | 133 | PF00069 | 0.513 |
MOD_CK1_1 | 266 | 272 | PF00069 | 0.523 |
MOD_CK1_1 | 290 | 296 | PF00069 | 0.630 |
MOD_CK1_1 | 383 | 389 | PF00069 | 0.440 |
MOD_CK1_1 | 43 | 49 | PF00069 | 0.661 |
MOD_CK1_1 | 65 | 71 | PF00069 | 0.776 |
MOD_CK2_1 | 13 | 19 | PF00069 | 0.309 |
MOD_CK2_1 | 148 | 154 | PF00069 | 0.518 |
MOD_CK2_1 | 173 | 179 | PF00069 | 0.592 |
MOD_CK2_1 | 279 | 285 | PF00069 | 0.521 |
MOD_CK2_1 | 407 | 413 | PF00069 | 0.463 |
MOD_Cter_Amidation | 2 | 5 | PF01082 | 0.506 |
MOD_DYRK1A_RPxSP_1 | 299 | 303 | PF00069 | 0.516 |
MOD_GlcNHglycan | 126 | 129 | PF01048 | 0.536 |
MOD_GlcNHglycan | 171 | 174 | PF01048 | 0.635 |
MOD_GlcNHglycan | 292 | 295 | PF01048 | 0.601 |
MOD_GlcNHglycan | 322 | 325 | PF01048 | 0.324 |
MOD_GlcNHglycan | 450 | 453 | PF01048 | 0.418 |
MOD_GlcNHglycan | 52 | 55 | PF01048 | 0.515 |
MOD_GSK3_1 | 123 | 130 | PF00069 | 0.495 |
MOD_GSK3_1 | 169 | 176 | PF00069 | 0.678 |
MOD_GSK3_1 | 218 | 225 | PF00069 | 0.485 |
MOD_GSK3_1 | 263 | 270 | PF00069 | 0.583 |
MOD_GSK3_1 | 277 | 284 | PF00069 | 0.604 |
MOD_GSK3_1 | 305 | 312 | PF00069 | 0.717 |
MOD_GSK3_1 | 316 | 323 | PF00069 | 0.418 |
MOD_GSK3_1 | 39 | 46 | PF00069 | 0.572 |
MOD_GSK3_1 | 407 | 414 | PF00069 | 0.490 |
MOD_GSK3_1 | 61 | 68 | PF00069 | 0.673 |
MOD_N-GLC_1 | 222 | 227 | PF02516 | 0.615 |
MOD_NEK2_1 | 320 | 325 | PF00069 | 0.375 |
MOD_NEK2_1 | 473 | 478 | PF00069 | 0.363 |
MOD_NEK2_2 | 13 | 18 | PF00069 | 0.366 |
MOD_NEK2_2 | 336 | 341 | PF00069 | 0.453 |
MOD_NEK2_2 | 521 | 526 | PF00069 | 0.402 |
MOD_PIKK_1 | 277 | 283 | PF00454 | 0.520 |
MOD_PKA_2 | 173 | 179 | PF00069 | 0.695 |
MOD_PKA_2 | 263 | 269 | PF00069 | 0.486 |
MOD_PKA_2 | 298 | 304 | PF00069 | 0.533 |
MOD_PKA_2 | 519 | 525 | PF00069 | 0.648 |
MOD_PKB_1 | 314 | 322 | PF00069 | 0.462 |
MOD_Plk_2-3 | 148 | 154 | PF00069 | 0.494 |
MOD_Plk_4 | 13 | 19 | PF00069 | 0.367 |
MOD_Plk_4 | 177 | 183 | PF00069 | 0.697 |
MOD_Plk_4 | 316 | 322 | PF00069 | 0.444 |
MOD_Plk_4 | 380 | 386 | PF00069 | 0.398 |
MOD_ProDKin_1 | 155 | 161 | PF00069 | 0.583 |
MOD_ProDKin_1 | 222 | 228 | PF00069 | 0.586 |
MOD_ProDKin_1 | 236 | 242 | PF00069 | 0.328 |
MOD_ProDKin_1 | 299 | 305 | PF00069 | 0.532 |
MOD_ProDKin_1 | 378 | 384 | PF00069 | 0.663 |
MOD_ProDKin_1 | 43 | 49 | PF00069 | 0.670 |
MOD_ProDKin_1 | 62 | 68 | PF00069 | 0.714 |
MOD_SUMO_rev_2 | 193 | 200 | PF00179 | 0.435 |
TRG_DiLeu_BaLyEn_6 | 204 | 209 | PF01217 | 0.467 |
TRG_DiLeu_BaLyEn_6 | 225 | 230 | PF01217 | 0.460 |
TRG_ENDOCYTIC_2 | 114 | 117 | PF00928 | 0.429 |
TRG_ENDOCYTIC_2 | 482 | 485 | PF00928 | 0.372 |
TRG_ER_diArg_1 | 205 | 207 | PF00400 | 0.510 |
TRG_ER_diArg_1 | 313 | 316 | PF00400 | 0.444 |
TRG_ER_diArg_1 | 490 | 492 | PF00400 | 0.525 |
TRG_ER_diArg_1 | 518 | 521 | PF00400 | 0.444 |
TRG_ER_diArg_1 | 88 | 91 | PF00400 | 0.496 |
TRG_ER_diArg_1 | 92 | 95 | PF00400 | 0.475 |
TRG_Pf-PMV_PEXEL_1 | 206 | 211 | PF00026 | 0.424 |
TRG_Pf-PMV_PEXEL_1 | 349 | 353 | PF00026 | 0.447 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IIC5 | Leptomonas seymouri | 47% | 100% |
A0A3S7WSX9 | Leishmania donovani | 69% | 100% |
A4HW02 | Leishmania infantum | 69% | 100% |
E9APQ4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 70% | 100% |
Q4QFS5 | Leishmania major | 69% | 96% |