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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 2 |
GO:0005968 | Rab-protein geranylgeranyltransferase complex | 4 | 12 |
GO:0032991 | protein-containing complex | 1 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:1902494 | catalytic complex | 2 | 12 |
GO:1990234 | transferase complex | 3 | 12 |
Related structures:
AlphaFold database: Q4Q488
Term | Name | Level | Count |
---|---|---|---|
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0018342 | protein prenylation | 4 | 12 |
GO:0018344 | protein geranylgeranylation | 5 | 12 |
GO:0019538 | protein metabolic process | 3 | 12 |
GO:0036211 | protein modification process | 4 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0043412 | macromolecule modification | 4 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0097354 | prenylation | 3 | 12 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004659 | prenyltransferase activity | 4 | 12 |
GO:0004661 | protein geranylgeranyltransferase activity | 4 | 12 |
GO:0004663 | Rab geranylgeranyltransferase activity | 5 | 12 |
GO:0008318 | protein prenyltransferase activity | 3 | 12 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0016765 | transferase activity, transferring alkyl or aryl (other than methyl) groups | 3 | 12 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 293 | 297 | PF00656 | 0.563 |
CLV_C14_Caspase3-7 | 352 | 356 | PF00656 | 0.393 |
CLV_NRD_NRD_1 | 104 | 106 | PF00675 | 0.443 |
CLV_NRD_NRD_1 | 174 | 176 | PF00675 | 0.451 |
CLV_NRD_NRD_1 | 198 | 200 | PF00675 | 0.242 |
CLV_NRD_NRD_1 | 344 | 346 | PF00675 | 0.504 |
CLV_NRD_NRD_1 | 424 | 426 | PF00675 | 0.467 |
CLV_NRD_NRD_1 | 456 | 458 | PF00675 | 0.468 |
CLV_NRD_NRD_1 | 473 | 475 | PF00675 | 0.515 |
CLV_NRD_NRD_1 | 68 | 70 | PF00675 | 0.353 |
CLV_PCSK_KEX2_1 | 103 | 105 | PF00082 | 0.472 |
CLV_PCSK_KEX2_1 | 198 | 200 | PF00082 | 0.242 |
CLV_PCSK_KEX2_1 | 258 | 260 | PF00082 | 0.219 |
CLV_PCSK_KEX2_1 | 344 | 346 | PF00082 | 0.500 |
CLV_PCSK_KEX2_1 | 424 | 426 | PF00082 | 0.457 |
CLV_PCSK_KEX2_1 | 455 | 457 | PF00082 | 0.482 |
CLV_PCSK_KEX2_1 | 473 | 475 | PF00082 | 0.543 |
CLV_PCSK_KEX2_1 | 68 | 70 | PF00082 | 0.353 |
CLV_PCSK_PC1ET2_1 | 258 | 260 | PF00082 | 0.190 |
CLV_PCSK_SKI1_1 | 117 | 121 | PF00082 | 0.303 |
CLV_PCSK_SKI1_1 | 199 | 203 | PF00082 | 0.258 |
CLV_PCSK_SKI1_1 | 305 | 309 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 32 | 36 | PF00082 | 0.481 |
CLV_PCSK_SKI1_1 | 425 | 429 | PF00082 | 0.503 |
CLV_PCSK_SKI1_1 | 69 | 73 | PF00082 | 0.341 |
CLV_PCSK_SKI1_1 | 9 | 13 | PF00082 | 0.606 |
DEG_APCC_DBOX_1 | 68 | 76 | PF00400 | 0.363 |
DEG_SPOP_SBC_1 | 231 | 235 | PF00917 | 0.655 |
DEG_SPOP_SBC_1 | 290 | 294 | PF00917 | 0.447 |
DEG_SPOP_SBC_1 | 89 | 93 | PF00917 | 0.584 |
DOC_PP2B_LxvP_1 | 56 | 59 | PF13499 | 0.486 |
DOC_PP4_FxxP_1 | 241 | 244 | PF00568 | 0.419 |
DOC_PP4_FxxP_1 | 334 | 337 | PF00568 | 0.469 |
DOC_USP7_MATH_1 | 221 | 225 | PF00917 | 0.642 |
DOC_USP7_MATH_1 | 231 | 235 | PF00917 | 0.693 |
DOC_USP7_MATH_1 | 273 | 277 | PF00917 | 0.513 |
DOC_USP7_MATH_1 | 74 | 78 | PF00917 | 0.535 |
DOC_USP7_MATH_1 | 89 | 93 | PF00917 | 0.619 |
DOC_USP7_UBL2_3 | 113 | 117 | PF12436 | 0.500 |
DOC_USP7_UBL2_3 | 5 | 9 | PF12436 | 0.667 |
DOC_WW_Pin1_4 | 10 | 15 | PF00397 | 0.623 |
DOC_WW_Pin1_4 | 217 | 222 | PF00397 | 0.664 |
DOC_WW_Pin1_4 | 233 | 238 | PF00397 | 0.683 |
DOC_WW_Pin1_4 | 240 | 245 | PF00397 | 0.460 |
LIG_14-3-3_CanoR_1 | 207 | 214 | PF00244 | 0.479 |
LIG_14-3-3_CanoR_1 | 376 | 385 | PF00244 | 0.571 |
LIG_14-3-3_CanoR_1 | 418 | 424 | PF00244 | 0.502 |
LIG_14-3-3_CanoR_1 | 425 | 431 | PF00244 | 0.416 |
LIG_Actin_WH2_1 | 305 | 322 | PF00022 | 0.315 |
LIG_APCC_ABBAyCdc20_2 | 320 | 326 | PF00400 | 0.526 |
LIG_APCC_ABBAyCdc20_2 | 473 | 479 | PF00400 | 0.502 |
LIG_BRCT_BRCA1_1 | 237 | 241 | PF00533 | 0.550 |
LIG_BRCT_BRCA1_1 | 330 | 334 | PF00533 | 0.448 |
LIG_Clathr_ClatBox_1 | 184 | 188 | PF01394 | 0.463 |
LIG_FHA_1 | 164 | 170 | PF00498 | 0.501 |
LIG_FHA_1 | 245 | 251 | PF00498 | 0.329 |
LIG_FHA_1 | 252 | 258 | PF00498 | 0.428 |
LIG_FHA_1 | 49 | 55 | PF00498 | 0.474 |
LIG_FHA_2 | 141 | 147 | PF00498 | 0.446 |
LIG_FHA_2 | 291 | 297 | PF00498 | 0.668 |
LIG_FHA_2 | 377 | 383 | PF00498 | 0.562 |
LIG_LIR_Apic_2 | 238 | 244 | PF02991 | 0.484 |
LIG_LIR_Apic_2 | 331 | 337 | PF02991 | 0.389 |
LIG_LIR_Gen_1 | 164 | 174 | PF02991 | 0.491 |
LIG_LIR_Nem_3 | 164 | 170 | PF02991 | 0.502 |
LIG_LIR_Nem_3 | 60 | 65 | PF02991 | 0.360 |
LIG_MLH1_MIPbox_1 | 238 | 242 | PF16413 | 0.486 |
LIG_NRBOX | 169 | 175 | PF00104 | 0.479 |
LIG_OCRL_FandH_1 | 128 | 140 | PF00620 | 0.538 |
LIG_OCRL_FandH_1 | 458 | 470 | PF00620 | 0.481 |
LIG_PCNA_yPIPBox_3 | 17 | 31 | PF02747 | 0.551 |
LIG_PCNA_yPIPBox_3 | 280 | 291 | PF02747 | 0.375 |
LIG_Pex14_2 | 334 | 338 | PF04695 | 0.469 |
LIG_SH2_CRK | 31 | 35 | PF00017 | 0.391 |
LIG_SH2_CRK | 67 | 71 | PF00017 | 0.398 |
LIG_SH2_STAP1 | 477 | 481 | PF00017 | 0.473 |
LIG_SH2_STAT5 | 252 | 255 | PF00017 | 0.522 |
LIG_SH2_STAT5 | 324 | 327 | PF00017 | 0.383 |
LIG_SH2_STAT5 | 347 | 350 | PF00017 | 0.456 |
LIG_SH2_STAT5 | 388 | 391 | PF00017 | 0.370 |
LIG_SH2_STAT5 | 461 | 464 | PF00017 | 0.456 |
LIG_SH2_STAT5 | 62 | 65 | PF00017 | 0.370 |
LIG_SH3_3 | 211 | 217 | PF00018 | 0.360 |
LIG_SH3_3 | 8 | 14 | PF00018 | 0.643 |
LIG_SUMO_SIM_anti_2 | 116 | 122 | PF11976 | 0.529 |
LIG_SUMO_SIM_par_1 | 54 | 60 | PF11976 | 0.472 |
LIG_TRAF2_1 | 20 | 23 | PF00917 | 0.446 |
LIG_TRAF2_1 | 243 | 246 | PF00917 | 0.552 |
LIG_TRAF2_1 | 358 | 361 | PF00917 | 0.402 |
LIG_UBA3_1 | 135 | 144 | PF00899 | 0.527 |
LIG_UBA3_1 | 169 | 176 | PF00899 | 0.483 |
MOD_CDK_SPxxK_3 | 10 | 17 | PF00069 | 0.611 |
MOD_CK1_1 | 232 | 238 | PF00069 | 0.615 |
MOD_CK1_1 | 262 | 268 | PF00069 | 0.441 |
MOD_CK1_1 | 401 | 407 | PF00069 | 0.539 |
MOD_CK1_1 | 419 | 425 | PF00069 | 0.544 |
MOD_CK1_1 | 84 | 90 | PF00069 | 0.709 |
MOD_CK2_1 | 140 | 146 | PF00069 | 0.455 |
MOD_CK2_1 | 240 | 246 | PF00069 | 0.438 |
MOD_CK2_1 | 273 | 279 | PF00069 | 0.460 |
MOD_CK2_1 | 376 | 382 | PF00069 | 0.553 |
MOD_CK2_1 | 84 | 90 | PF00069 | 0.680 |
MOD_GlcNHglycan | 223 | 226 | PF01048 | 0.612 |
MOD_GlcNHglycan | 238 | 241 | PF01048 | 0.582 |
MOD_GlcNHglycan | 264 | 267 | PF01048 | 0.252 |
MOD_GlcNHglycan | 275 | 278 | PF01048 | 0.350 |
MOD_GlcNHglycan | 329 | 333 | PF01048 | 0.308 |
MOD_GlcNHglycan | 411 | 414 | PF01048 | 0.668 |
MOD_GlcNHglycan | 419 | 422 | PF01048 | 0.476 |
MOD_GlcNHglycan | 439 | 442 | PF01048 | 0.601 |
MOD_GlcNHglycan | 83 | 87 | PF01048 | 0.700 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.620 |
MOD_GSK3_1 | 217 | 224 | PF00069 | 0.606 |
MOD_GSK3_1 | 226 | 233 | PF00069 | 0.671 |
MOD_GSK3_1 | 236 | 243 | PF00069 | 0.526 |
MOD_GSK3_1 | 30 | 37 | PF00069 | 0.423 |
MOD_GSK3_1 | 401 | 408 | PF00069 | 0.572 |
MOD_GSK3_1 | 433 | 440 | PF00069 | 0.526 |
MOD_GSK3_1 | 44 | 51 | PF00069 | 0.390 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.707 |
MOD_N-GLC_1 | 159 | 164 | PF02516 | 0.608 |
MOD_N-GLC_1 | 259 | 264 | PF02516 | 0.261 |
MOD_N-GLC_1 | 43 | 48 | PF02516 | 0.502 |
MOD_NEK2_1 | 169 | 174 | PF00069 | 0.376 |
MOD_NEK2_1 | 206 | 211 | PF00069 | 0.480 |
MOD_NEK2_1 | 250 | 255 | PF00069 | 0.457 |
MOD_NEK2_1 | 30 | 35 | PF00069 | 0.452 |
MOD_NEK2_1 | 359 | 364 | PF00069 | 0.478 |
MOD_NEK2_1 | 437 | 442 | PF00069 | 0.404 |
MOD_PIKK_1 | 206 | 212 | PF00454 | 0.420 |
MOD_PIKK_1 | 226 | 232 | PF00454 | 0.622 |
MOD_PIKK_1 | 398 | 404 | PF00454 | 0.554 |
MOD_PKA_2 | 206 | 212 | PF00069 | 0.544 |
MOD_PKA_2 | 375 | 381 | PF00069 | 0.358 |
MOD_PKA_2 | 417 | 423 | PF00069 | 0.515 |
MOD_Plk_1 | 262 | 268 | PF00069 | 0.447 |
MOD_Plk_1 | 328 | 334 | PF00069 | 0.364 |
MOD_Plk_1 | 359 | 365 | PF00069 | 0.501 |
MOD_Plk_1 | 43 | 49 | PF00069 | 0.431 |
MOD_Plk_4 | 169 | 175 | PF00069 | 0.465 |
MOD_Plk_4 | 30 | 36 | PF00069 | 0.414 |
MOD_Plk_4 | 359 | 365 | PF00069 | 0.457 |
MOD_Plk_4 | 433 | 439 | PF00069 | 0.532 |
MOD_Plk_4 | 60 | 66 | PF00069 | 0.364 |
MOD_ProDKin_1 | 10 | 16 | PF00069 | 0.615 |
MOD_ProDKin_1 | 217 | 223 | PF00069 | 0.669 |
MOD_ProDKin_1 | 233 | 239 | PF00069 | 0.676 |
MOD_ProDKin_1 | 240 | 246 | PF00069 | 0.453 |
MOD_SUMO_rev_2 | 13 | 19 | PF00179 | 0.530 |
TRG_DiLeu_BaEn_2 | 313 | 319 | PF01217 | 0.459 |
TRG_DiLeu_BaEn_4 | 245 | 251 | PF01217 | 0.451 |
TRG_ENDOCYTIC_2 | 126 | 129 | PF00928 | 0.442 |
TRG_ENDOCYTIC_2 | 167 | 170 | PF00928 | 0.524 |
TRG_ENDOCYTIC_2 | 31 | 34 | PF00928 | 0.400 |
TRG_ENDOCYTIC_2 | 335 | 338 | PF00928 | 0.339 |
TRG_ENDOCYTIC_2 | 388 | 391 | PF00928 | 0.387 |
TRG_ENDOCYTIC_2 | 477 | 480 | PF00928 | 0.356 |
TRG_ENDOCYTIC_2 | 67 | 70 | PF00928 | 0.303 |
TRG_ER_diArg_1 | 102 | 105 | PF00400 | 0.397 |
TRG_ER_diArg_1 | 197 | 199 | PF00400 | 0.442 |
TRG_ER_diArg_1 | 343 | 345 | PF00400 | 0.490 |
TRG_ER_diArg_1 | 423 | 425 | PF00400 | 0.306 |
TRG_ER_diArg_1 | 455 | 457 | PF00400 | 0.470 |
TRG_ER_diArg_1 | 472 | 474 | PF00400 | 0.553 |
TRG_ER_diArg_1 | 67 | 69 | PF00400 | 0.353 |
TRG_Pf-PMV_PEXEL_1 | 474 | 478 | PF00026 | 0.528 |
TRG_Pf-PMV_PEXEL_1 | 68 | 73 | PF00026 | 0.440 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I6W4 | Leptomonas seymouri | 51% | 100% |
A0A0S4JI96 | Bodo saltans | 28% | 100% |
A0A1X0P0V1 | Trypanosomatidae | 27% | 88% |
A0A3S7X6L4 | Leishmania donovani | 89% | 100% |
A0A422P2I9 | Trypanosoma rangeli | 32% | 97% |
A4HLF6 | Leishmania braziliensis | 74% | 100% |
A4I8W7 | Leishmania infantum | 89% | 100% |
A5A779 | Sus scrofa | 25% | 86% |
D0A4W1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
E9B3T6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
O93829 | Candida albicans | 24% | 100% |
Q08602 | Rattus norvegicus | 25% | 86% |
Q5EA80 | Bos taurus | 24% | 86% |
Q5NVK5 | Pongo abelii | 27% | 86% |
Q92696 | Homo sapiens | 27% | 86% |
Q9JHK4 | Mus musculus | 26% | 86% |
V5BJU9 | Trypanosoma cruzi | 35% | 100% |