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:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9AX36
Term | Name | Level | Count |
---|---|---|---|
GO:0006807 | nitrogen compound metabolic process | 2 | 3 |
GO:0008152 | metabolic process | 1 | 3 |
GO:0009987 | cellular process | 1 | 3 |
GO:0018342 | protein prenylation | 4 | 3 |
GO:0019538 | protein metabolic process | 3 | 3 |
GO:0036211 | protein modification process | 4 | 3 |
GO:0043170 | macromolecule metabolic process | 3 | 3 |
GO:0043412 | macromolecule modification | 4 | 3 |
GO:0044237 | cellular metabolic process | 2 | 3 |
GO:0044238 | primary metabolic process | 2 | 3 |
GO:0071704 | organic substance metabolic process | 2 | 3 |
GO:0097354 | prenylation | 3 | 3 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 3 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 4 |
GO:0004659 | prenyltransferase activity | 4 | 3 |
GO:0008318 | protein prenyltransferase activity | 3 | 3 |
GO:0016740 | transferase activity | 2 | 4 |
GO:0016765 | transferase activity, transferring alkyl or aryl (other than methyl) groups | 3 | 3 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 437 | 441 | PF00656 | 0.668 |
CLV_NRD_NRD_1 | 151 | 153 | PF00675 | 0.416 |
CLV_NRD_NRD_1 | 253 | 255 | PF00675 | 0.375 |
CLV_NRD_NRD_1 | 313 | 315 | PF00675 | 0.538 |
CLV_NRD_NRD_1 | 338 | 340 | PF00675 | 0.735 |
CLV_NRD_NRD_1 | 79 | 81 | PF00675 | 0.538 |
CLV_PCSK_KEX2_1 | 150 | 152 | PF00082 | 0.403 |
CLV_PCSK_KEX2_1 | 253 | 255 | PF00082 | 0.377 |
CLV_PCSK_KEX2_1 | 338 | 340 | PF00082 | 0.735 |
CLV_PCSK_KEX2_1 | 79 | 81 | PF00082 | 0.545 |
CLV_PCSK_SKI1_1 | 122 | 126 | PF00082 | 0.573 |
CLV_PCSK_SKI1_1 | 364 | 368 | PF00082 | 0.505 |
CLV_PCSK_SKI1_1 | 39 | 43 | PF00082 | 0.494 |
CLV_PCSK_SKI1_1 | 86 | 90 | PF00082 | 0.449 |
DEG_APCC_DBOX_1 | 121 | 129 | PF00400 | 0.587 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.581 |
DEG_ODPH_VHL_1 | 367 | 378 | PF01847 | 0.541 |
DEG_SPOP_SBC_1 | 64 | 68 | PF00917 | 0.556 |
DOC_CKS1_1 | 30 | 35 | PF01111 | 0.443 |
DOC_CYCLIN_RxL_1 | 170 | 182 | PF00134 | 0.225 |
DOC_CYCLIN_yCln2_LP_2 | 442 | 448 | PF00134 | 0.666 |
DOC_MAPK_MEF2A_6 | 176 | 185 | PF00069 | 0.421 |
DOC_PP1_RVXF_1 | 251 | 258 | PF00149 | 0.405 |
DOC_USP7_MATH_1 | 262 | 266 | PF00917 | 0.579 |
DOC_USP7_MATH_1 | 410 | 414 | PF00917 | 0.516 |
DOC_USP7_MATH_1 | 461 | 465 | PF00917 | 0.519 |
DOC_USP7_MATH_1 | 48 | 52 | PF00917 | 0.578 |
DOC_WW_Pin1_4 | 107 | 112 | PF00397 | 0.700 |
DOC_WW_Pin1_4 | 114 | 119 | PF00397 | 0.541 |
DOC_WW_Pin1_4 | 29 | 34 | PF00397 | 0.442 |
DOC_WW_Pin1_4 | 406 | 411 | PF00397 | 0.582 |
DOC_WW_Pin1_4 | 441 | 446 | PF00397 | 0.638 |
LIG_14-3-3_CanoR_1 | 122 | 132 | PF00244 | 0.483 |
LIG_14-3-3_CanoR_1 | 198 | 204 | PF00244 | 0.371 |
LIG_14-3-3_CanoR_1 | 425 | 431 | PF00244 | 0.443 |
LIG_Actin_WH2_2 | 142 | 157 | PF00022 | 0.468 |
LIG_Actin_WH2_2 | 410 | 427 | PF00022 | 0.562 |
LIG_APCC_ABBA_1 | 383 | 388 | PF00400 | 0.319 |
LIG_CaM_IQ_9 | 376 | 391 | PF13499 | 0.543 |
LIG_Clathr_ClatBox_1 | 178 | 182 | PF01394 | 0.205 |
LIG_EH1_1 | 172 | 180 | PF00400 | 0.224 |
LIG_eIF4E_1 | 430 | 436 | PF01652 | 0.533 |
LIG_FHA_1 | 102 | 108 | PF00498 | 0.648 |
LIG_FHA_1 | 155 | 161 | PF00498 | 0.288 |
LIG_FHA_1 | 297 | 303 | PF00498 | 0.442 |
LIG_FHA_2 | 11 | 17 | PF00498 | 0.475 |
LIG_FHA_2 | 377 | 383 | PF00498 | 0.476 |
LIG_FHA_2 | 427 | 433 | PF00498 | 0.376 |
LIG_FXI_DFP_1 | 70 | 74 | PF00024 | 0.504 |
LIG_LIR_Gen_1 | 144 | 154 | PF02991 | 0.536 |
LIG_LIR_Gen_1 | 182 | 191 | PF02991 | 0.232 |
LIG_LIR_Gen_1 | 2 | 12 | PF02991 | 0.543 |
LIG_LIR_Gen_1 | 299 | 306 | PF02991 | 0.380 |
LIG_LIR_Gen_1 | 428 | 436 | PF02991 | 0.400 |
LIG_LIR_Gen_1 | 459 | 470 | PF02991 | 0.467 |
LIG_LIR_Gen_1 | 67 | 77 | PF02991 | 0.521 |
LIG_LIR_Nem_3 | 144 | 149 | PF02991 | 0.538 |
LIG_LIR_Nem_3 | 182 | 187 | PF02991 | 0.504 |
LIG_LIR_Nem_3 | 2 | 8 | PF02991 | 0.556 |
LIG_LIR_Nem_3 | 299 | 304 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 428 | 433 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 459 | 465 | PF02991 | 0.493 |
LIG_LIR_Nem_3 | 67 | 73 | PF02991 | 0.545 |
LIG_NRBOX | 301 | 307 | PF00104 | 0.424 |
LIG_NRBOX | 473 | 479 | PF00104 | 0.491 |
LIG_Pex14_1 | 426 | 430 | PF04695 | 0.524 |
LIG_Pex14_2 | 449 | 453 | PF04695 | 0.375 |
LIG_Pex14_2 | 89 | 93 | PF04695 | 0.548 |
LIG_RPA_C_Fungi | 75 | 87 | PF08784 | 0.461 |
LIG_SH2_CRK | 208 | 212 | PF00017 | 0.270 |
LIG_SH2_CRK | 252 | 256 | PF00017 | 0.465 |
LIG_SH2_CRK | 5 | 9 | PF00017 | 0.556 |
LIG_SH2_NCK_1 | 5 | 9 | PF00017 | 0.556 |
LIG_SH2_PTP2 | 430 | 433 | PF00017 | 0.537 |
LIG_SH2_STAP1 | 5 | 9 | PF00017 | 0.556 |
LIG_SH2_STAT3 | 470 | 473 | PF00017 | 0.442 |
LIG_SH2_STAT5 | 26 | 29 | PF00017 | 0.548 |
LIG_SH2_STAT5 | 301 | 304 | PF00017 | 0.395 |
LIG_SH2_STAT5 | 430 | 433 | PF00017 | 0.481 |
LIG_SH2_STAT5 | 5 | 8 | PF00017 | 0.553 |
LIG_SH2_STAT5 | 70 | 73 | PF00017 | 0.267 |
LIG_SH3_3 | 30 | 36 | PF00018 | 0.586 |
LIG_SUMO_SIM_anti_2 | 177 | 182 | PF11976 | 0.276 |
LIG_SUMO_SIM_par_1 | 177 | 182 | PF11976 | 0.246 |
LIG_SUMO_SIM_par_1 | 413 | 419 | PF11976 | 0.564 |
LIG_UBA3_1 | 183 | 192 | PF00899 | 0.489 |
LIG_WRC_WIRS_1 | 90 | 95 | PF05994 | 0.545 |
MOD_CK1_1 | 110 | 116 | PF00069 | 0.650 |
MOD_CK1_1 | 29 | 35 | PF00069 | 0.511 |
MOD_CK1_1 | 296 | 302 | PF00069 | 0.431 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.526 |
MOD_CK1_1 | 413 | 419 | PF00069 | 0.546 |
MOD_CK1_1 | 444 | 450 | PF00069 | 0.594 |
MOD_CK1_1 | 454 | 460 | PF00069 | 0.522 |
MOD_CK2_1 | 190 | 196 | PF00069 | 0.454 |
MOD_CK2_1 | 376 | 382 | PF00069 | 0.413 |
MOD_CK2_1 | 426 | 432 | PF00069 | 0.467 |
MOD_CK2_1 | 479 | 485 | PF00069 | 0.378 |
MOD_GlcNHglycan | 166 | 169 | PF01048 | 0.529 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.486 |
MOD_GlcNHglycan | 262 | 265 | PF01048 | 0.475 |
MOD_GlcNHglycan | 295 | 299 | PF01048 | 0.376 |
MOD_GlcNHglycan | 320 | 323 | PF01048 | 0.510 |
MOD_GlcNHglycan | 339 | 342 | PF01048 | 0.725 |
MOD_GlcNHglycan | 353 | 356 | PF01048 | 0.589 |
MOD_GlcNHglycan | 364 | 367 | PF01048 | 0.327 |
MOD_GlcNHglycan | 418 | 421 | PF01048 | 0.578 |
MOD_GlcNHglycan | 446 | 449 | PF01048 | 0.567 |
MOD_GlcNHglycan | 455 | 459 | PF01048 | 0.427 |
MOD_GSK3_1 | 110 | 117 | PF00069 | 0.685 |
MOD_GSK3_1 | 154 | 161 | PF00069 | 0.386 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.423 |
MOD_GSK3_1 | 406 | 413 | PF00069 | 0.500 |
MOD_GSK3_1 | 453 | 460 | PF00069 | 0.494 |
MOD_GSK3_1 | 461 | 468 | PF00069 | 0.375 |
MOD_GSK3_1 | 64 | 71 | PF00069 | 0.551 |
MOD_N-GLC_1 | 465 | 470 | PF02516 | 0.532 |
MOD_N-GLC_1 | 479 | 484 | PF02516 | 0.415 |
MOD_N-GLC_2 | 204 | 206 | PF02516 | 0.443 |
MOD_NEK2_1 | 154 | 159 | PF00069 | 0.423 |
MOD_NEK2_1 | 183 | 188 | PF00069 | 0.480 |
MOD_NEK2_1 | 260 | 265 | PF00069 | 0.351 |
MOD_NEK2_1 | 337 | 342 | PF00069 | 0.687 |
MOD_NEK2_1 | 371 | 376 | PF00069 | 0.415 |
MOD_NEK2_1 | 42 | 47 | PF00069 | 0.571 |
MOD_NEK2_1 | 465 | 470 | PF00069 | 0.484 |
MOD_NEK2_1 | 478 | 483 | PF00069 | 0.518 |
MOD_OFUCOSY | 56 | 62 | PF10250 | 0.381 |
MOD_PIKK_1 | 376 | 382 | PF00454 | 0.448 |
MOD_PIKK_1 | 42 | 48 | PF00454 | 0.515 |
MOD_PKA_2 | 154 | 160 | PF00069 | 0.467 |
MOD_PKA_2 | 337 | 343 | PF00069 | 0.681 |
MOD_PKA_2 | 478 | 484 | PF00069 | 0.644 |
MOD_Plk_1 | 316 | 322 | PF00069 | 0.646 |
MOD_Plk_1 | 410 | 416 | PF00069 | 0.477 |
MOD_Plk_1 | 465 | 471 | PF00069 | 0.509 |
MOD_Plk_1 | 58 | 64 | PF00069 | 0.471 |
MOD_Plk_2-3 | 10 | 16 | PF00069 | 0.255 |
MOD_Plk_4 | 128 | 134 | PF00069 | 0.432 |
MOD_Plk_4 | 190 | 196 | PF00069 | 0.441 |
MOD_Plk_4 | 297 | 303 | PF00069 | 0.394 |
MOD_Plk_4 | 3 | 9 | PF00069 | 0.557 |
MOD_Plk_4 | 410 | 416 | PF00069 | 0.660 |
MOD_Plk_4 | 426 | 432 | PF00069 | 0.348 |
MOD_Plk_4 | 473 | 479 | PF00069 | 0.508 |
MOD_ProDKin_1 | 107 | 113 | PF00069 | 0.693 |
MOD_ProDKin_1 | 114 | 120 | PF00069 | 0.525 |
MOD_ProDKin_1 | 29 | 35 | PF00069 | 0.438 |
MOD_ProDKin_1 | 406 | 412 | PF00069 | 0.590 |
MOD_ProDKin_1 | 441 | 447 | PF00069 | 0.632 |
MOD_SUMO_rev_2 | 156 | 165 | PF00179 | 0.607 |
TRG_ENDOCYTIC_2 | 208 | 211 | PF00928 | 0.270 |
TRG_ENDOCYTIC_2 | 252 | 255 | PF00928 | 0.502 |
TRG_ENDOCYTIC_2 | 301 | 304 | PF00928 | 0.395 |
TRG_ENDOCYTIC_2 | 430 | 433 | PF00928 | 0.490 |
TRG_ENDOCYTIC_2 | 5 | 8 | PF00928 | 0.553 |
TRG_ENDOCYTIC_2 | 70 | 73 | PF00928 | 0.267 |
TRG_ER_diArg_1 | 149 | 152 | PF00400 | 0.426 |
TRG_ER_diArg_1 | 252 | 254 | PF00400 | 0.366 |
TRG_ER_diArg_1 | 337 | 339 | PF00400 | 0.735 |
TRG_ER_diArg_1 | 79 | 81 | PF00400 | 0.535 |
TRG_NES_CRM1_1 | 169 | 182 | PF08389 | 0.512 |
TRG_Pf-PMV_PEXEL_1 | 152 | 156 | PF00026 | 0.477 |
TRG_Pf-PMV_PEXEL_1 | 192 | 196 | PF00026 | 0.486 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HTJ1 | Leptomonas seymouri | 41% | 100% |
A0A0S4JLJ0 | Bodo saltans | 26% | 100% |
A0A1X0NWB3 | Trypanosomatidae | 25% | 100% |
A0A3Q8IF02 | Leishmania donovani | 84% | 100% |
A0A422NWV9 | Trypanosoma rangeli | 30% | 100% |
A4HDQ2 | Leishmania braziliensis | 72% | 100% |
A4I0Z8 | Leishmania infantum | 85% | 100% |
C9ZWB1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
Q4QAE0 | Leishmania major | 82% | 100% |