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: A4HDQ2
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 | 314 | 318 | PF00656 | 0.429 |
CLV_NRD_NRD_1 | 151 | 153 | PF00675 | 0.344 |
CLV_NRD_NRD_1 | 253 | 255 | PF00675 | 0.315 |
CLV_NRD_NRD_1 | 339 | 341 | PF00675 | 0.746 |
CLV_NRD_NRD_1 | 354 | 356 | PF00675 | 0.462 |
CLV_NRD_NRD_1 | 384 | 386 | PF00675 | 0.454 |
CLV_PCSK_KEX2_1 | 150 | 152 | PF00082 | 0.333 |
CLV_PCSK_KEX2_1 | 253 | 255 | PF00082 | 0.316 |
CLV_PCSK_KEX2_1 | 339 | 341 | PF00082 | 0.746 |
CLV_PCSK_KEX2_1 | 384 | 386 | PF00082 | 0.479 |
CLV_PCSK_SKI1_1 | 122 | 126 | PF00082 | 0.528 |
CLV_PCSK_SKI1_1 | 39 | 43 | PF00082 | 0.421 |
CLV_PCSK_SKI1_1 | 86 | 90 | PF00082 | 0.365 |
CLV_PCSK_SKI1_1 | 97 | 101 | PF00082 | 0.474 |
DEG_APCC_DBOX_1 | 121 | 129 | PF00400 | 0.437 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.470 |
DEG_ODPH_VHL_1 | 367 | 378 | PF01847 | 0.414 |
DEG_SCF_FBW7_1 | 114 | 121 | PF00400 | 0.352 |
DEG_SPOP_SBC_1 | 64 | 68 | PF00917 | 0.454 |
DOC_CKS1_1 | 30 | 35 | PF01111 | 0.361 |
DOC_CYCLIN_RxL_1 | 250 | 259 | PF00134 | 0.327 |
DOC_CYCLIN_RxL_1 | 408 | 421 | PF00134 | 0.349 |
DOC_CYCLIN_yCln2_LP_2 | 442 | 448 | PF00134 | 0.523 |
DOC_MAPK_gen_1 | 253 | 262 | PF00069 | 0.331 |
DOC_MAPK_MEF2A_6 | 176 | 185 | PF00069 | 0.397 |
DOC_MAPK_MEF2A_6 | 256 | 264 | PF00069 | 0.266 |
DOC_PP1_RVXF_1 | 251 | 258 | PF00149 | 0.322 |
DOC_PP1_SILK_1 | 475 | 480 | PF00149 | 0.287 |
DOC_USP7_MATH_1 | 461 | 465 | PF00917 | 0.474 |
DOC_USP7_MATH_1 | 84 | 88 | PF00917 | 0.490 |
DOC_USP7_UBL2_3 | 356 | 360 | PF12436 | 0.451 |
DOC_WW_Pin1_4 | 114 | 119 | PF00397 | 0.541 |
DOC_WW_Pin1_4 | 29 | 34 | PF00397 | 0.417 |
DOC_WW_Pin1_4 | 326 | 331 | PF00397 | 0.460 |
DOC_WW_Pin1_4 | 359 | 364 | PF00397 | 0.453 |
DOC_WW_Pin1_4 | 406 | 411 | PF00397 | 0.443 |
DOC_WW_Pin1_4 | 441 | 446 | PF00397 | 0.622 |
LIG_14-3-3_CanoR_1 | 256 | 261 | PF00244 | 0.360 |
LIG_14-3-3_CanoR_1 | 339 | 346 | PF00244 | 0.502 |
LIG_14-3-3_CanoR_1 | 355 | 364 | PF00244 | 0.738 |
LIG_14-3-3_CanoR_1 | 413 | 418 | PF00244 | 0.430 |
LIG_14-3-3_CanoR_1 | 425 | 431 | PF00244 | 0.494 |
LIG_14-3-3_CanoR_1 | 432 | 442 | PF00244 | 0.570 |
LIG_14-3-3_CanoR_1 | 479 | 483 | PF00244 | 0.634 |
LIG_14-3-3_CanoR_1 | 79 | 89 | PF00244 | 0.240 |
LIG_14-3-3_CanoR_1 | 95 | 103 | PF00244 | 0.358 |
LIG_Actin_WH2_2 | 410 | 427 | PF00022 | 0.448 |
LIG_AP2alpha_1 | 89 | 93 | PF02296 | 0.248 |
LIG_CaM_IQ_9 | 376 | 391 | PF13499 | 0.508 |
LIG_FHA_1 | 115 | 121 | PF00498 | 0.479 |
LIG_FHA_1 | 220 | 226 | PF00498 | 0.327 |
LIG_FHA_1 | 257 | 263 | PF00498 | 0.360 |
LIG_FHA_1 | 321 | 327 | PF00498 | 0.523 |
LIG_FHA_1 | 58 | 64 | PF00498 | 0.385 |
LIG_FHA_1 | 66 | 72 | PF00498 | 0.388 |
LIG_FHA_2 | 312 | 318 | PF00498 | 0.359 |
LIG_FHA_2 | 377 | 383 | PF00498 | 0.473 |
LIG_FHA_2 | 434 | 440 | PF00498 | 0.433 |
LIG_GBD_Chelix_1 | 474 | 482 | PF00786 | 0.290 |
LIG_LIR_Gen_1 | 144 | 154 | PF02991 | 0.521 |
LIG_LIR_Gen_1 | 177 | 185 | PF02991 | 0.329 |
LIG_LIR_Gen_1 | 2 | 12 | PF02991 | 0.420 |
LIG_LIR_Gen_1 | 300 | 307 | PF02991 | 0.324 |
LIG_LIR_Gen_1 | 427 | 435 | PF02991 | 0.349 |
LIG_LIR_Gen_1 | 459 | 470 | PF02991 | 0.402 |
LIG_LIR_Nem_3 | 144 | 149 | PF02991 | 0.525 |
LIG_LIR_Nem_3 | 177 | 181 | PF02991 | 0.327 |
LIG_LIR_Nem_3 | 182 | 187 | PF02991 | 0.357 |
LIG_LIR_Nem_3 | 2 | 8 | PF02991 | 0.432 |
LIG_LIR_Nem_3 | 300 | 304 | PF02991 | 0.324 |
LIG_LIR_Nem_3 | 427 | 433 | PF02991 | 0.410 |
LIG_LIR_Nem_3 | 459 | 465 | PF02991 | 0.427 |
LIG_LIR_Nem_3 | 72 | 76 | PF02991 | 0.443 |
LIG_NRBOX | 301 | 307 | PF00104 | 0.346 |
LIG_OCRL_FandH_1 | 256 | 268 | PF00620 | 0.302 |
LIG_PAM2_1 | 128 | 140 | PF00658 | 0.222 |
LIG_PCNA_PIPBox_1 | 411 | 420 | PF02747 | 0.479 |
LIG_PCNA_yPIPBox_3 | 408 | 418 | PF02747 | 0.479 |
LIG_Pex14_1 | 426 | 430 | PF04695 | 0.491 |
LIG_Pex14_2 | 149 | 153 | PF04695 | 0.234 |
LIG_Pex14_2 | 184 | 188 | PF04695 | 0.231 |
LIG_Pex14_2 | 89 | 93 | PF04695 | 0.396 |
LIG_PTB_Apo_2 | 211 | 218 | PF02174 | 0.442 |
LIG_PTB_Phospho_1 | 211 | 217 | PF10480 | 0.349 |
LIG_SH2_CRK | 252 | 256 | PF00017 | 0.427 |
LIG_SH2_CRK | 430 | 434 | PF00017 | 0.400 |
LIG_SH2_CRK | 5 | 9 | PF00017 | 0.413 |
LIG_SH2_NCK_1 | 5 | 9 | PF00017 | 0.413 |
LIG_SH2_SRC | 217 | 220 | PF00017 | 0.400 |
LIG_SH2_STAP1 | 307 | 311 | PF00017 | 0.355 |
LIG_SH2_STAP1 | 5 | 9 | PF00017 | 0.413 |
LIG_SH2_STAT3 | 470 | 473 | PF00017 | 0.379 |
LIG_SH2_STAT5 | 172 | 175 | PF00017 | 0.264 |
LIG_SH2_STAT5 | 217 | 220 | PF00017 | 0.400 |
LIG_SH2_STAT5 | 26 | 29 | PF00017 | 0.399 |
LIG_SH2_STAT5 | 301 | 304 | PF00017 | 0.317 |
LIG_SH2_STAT5 | 5 | 8 | PF00017 | 0.409 |
LIG_SUMO_SIM_par_1 | 412 | 419 | PF11976 | 0.460 |
LIG_SUMO_SIM_par_1 | 72 | 78 | PF11976 | 0.347 |
LIG_TRAF2_1 | 48 | 51 | PF00917 | 0.359 |
LIG_TRFH_1 | 44 | 48 | PF08558 | 0.383 |
LIG_UBA3_1 | 183 | 192 | PF00899 | 0.450 |
LIG_WRC_WIRS_1 | 146 | 151 | PF05994 | 0.357 |
LIG_WRC_WIRS_1 | 85 | 90 | PF05994 | 0.349 |
MOD_CDK_SPxxK_3 | 406 | 413 | PF00069 | 0.377 |
MOD_CK1_1 | 29 | 35 | PF00069 | 0.535 |
MOD_CK1_1 | 297 | 303 | PF00069 | 0.390 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.475 |
MOD_CK1_1 | 359 | 365 | PF00069 | 0.630 |
MOD_CK1_1 | 409 | 415 | PF00069 | 0.538 |
MOD_CK1_1 | 416 | 422 | PF00069 | 0.549 |
MOD_CK1_1 | 444 | 450 | PF00069 | 0.561 |
MOD_CK1_1 | 454 | 460 | PF00069 | 0.498 |
MOD_CK2_1 | 190 | 196 | PF00069 | 0.452 |
MOD_CK2_1 | 376 | 382 | PF00069 | 0.364 |
MOD_CK2_1 | 433 | 439 | PF00069 | 0.515 |
MOD_GlcNHglycan | 20 | 23 | PF01048 | 0.284 |
MOD_GlcNHglycan | 295 | 299 | PF01048 | 0.327 |
MOD_GlcNHglycan | 418 | 421 | PF01048 | 0.483 |
MOD_GlcNHglycan | 446 | 449 | PF01048 | 0.524 |
MOD_GlcNHglycan | 455 | 459 | PF01048 | 0.379 |
MOD_GlcNHglycan | 97 | 100 | PF01048 | 0.551 |
MOD_GSK3_1 | 110 | 117 | PF00069 | 0.651 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.397 |
MOD_GSK3_1 | 322 | 329 | PF00069 | 0.733 |
MOD_GSK3_1 | 351 | 358 | PF00069 | 0.621 |
MOD_GSK3_1 | 409 | 416 | PF00069 | 0.497 |
MOD_GSK3_1 | 453 | 460 | PF00069 | 0.435 |
MOD_GSK3_1 | 461 | 468 | PF00069 | 0.332 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.370 |
MOD_N-GLC_1 | 262 | 267 | PF02516 | 0.393 |
MOD_N-GLC_1 | 465 | 470 | PF02516 | 0.510 |
MOD_N-GLC_2 | 204 | 206 | PF02516 | 0.331 |
MOD_NEK2_1 | 183 | 188 | PF00069 | 0.330 |
MOD_NEK2_1 | 371 | 376 | PF00069 | 0.361 |
MOD_NEK2_1 | 42 | 47 | PF00069 | 0.557 |
MOD_NEK2_1 | 424 | 429 | PF00069 | 0.329 |
MOD_NEK2_1 | 465 | 470 | PF00069 | 0.445 |
MOD_NEK2_1 | 478 | 483 | PF00069 | 0.450 |
MOD_NEK2_1 | 57 | 62 | PF00069 | 0.511 |
MOD_NEK2_1 | 89 | 94 | PF00069 | 0.412 |
MOD_NEK2_2 | 26 | 31 | PF00069 | 0.361 |
MOD_NEK2_2 | 84 | 89 | PF00069 | 0.232 |
MOD_OFUCOSY | 202 | 208 | PF10250 | 0.244 |
MOD_OFUCOSY | 56 | 62 | PF10250 | 0.340 |
MOD_PIKK_1 | 165 | 171 | PF00454 | 0.367 |
MOD_PIKK_1 | 376 | 382 | PF00454 | 0.435 |
MOD_PKA_1 | 339 | 345 | PF00069 | 0.502 |
MOD_PKA_1 | 355 | 361 | PF00069 | 0.449 |
MOD_PKA_1 | 384 | 390 | PF00069 | 0.444 |
MOD_PKA_2 | 339 | 345 | PF00069 | 0.639 |
MOD_PKA_2 | 384 | 390 | PF00069 | 0.444 |
MOD_PKA_2 | 424 | 430 | PF00069 | 0.326 |
MOD_PKA_2 | 478 | 484 | PF00069 | 0.630 |
MOD_PKB_1 | 254 | 262 | PF00069 | 0.369 |
MOD_Plk_1 | 232 | 238 | PF00069 | 0.392 |
MOD_Plk_1 | 3 | 9 | PF00069 | 0.298 |
MOD_Plk_1 | 465 | 471 | PF00069 | 0.495 |
MOD_Plk_1 | 58 | 64 | PF00069 | 0.539 |
MOD_Plk_4 | 128 | 134 | PF00069 | 0.386 |
MOD_Plk_4 | 183 | 189 | PF00069 | 0.305 |
MOD_Plk_4 | 190 | 196 | PF00069 | 0.361 |
MOD_Plk_4 | 232 | 238 | PF00069 | 0.233 |
MOD_Plk_4 | 297 | 303 | PF00069 | 0.366 |
MOD_Plk_4 | 3 | 9 | PF00069 | 0.543 |
MOD_Plk_4 | 322 | 328 | PF00069 | 0.524 |
MOD_Plk_4 | 371 | 377 | PF00069 | 0.403 |
MOD_Plk_4 | 413 | 419 | PF00069 | 0.458 |
MOD_Plk_4 | 473 | 479 | PF00069 | 0.469 |
MOD_ProDKin_1 | 114 | 120 | PF00069 | 0.528 |
MOD_ProDKin_1 | 29 | 35 | PF00069 | 0.415 |
MOD_ProDKin_1 | 326 | 332 | PF00069 | 0.464 |
MOD_ProDKin_1 | 359 | 365 | PF00069 | 0.445 |
MOD_ProDKin_1 | 406 | 412 | PF00069 | 0.448 |
MOD_ProDKin_1 | 441 | 447 | PF00069 | 0.616 |
MOD_SUMO_rev_2 | 156 | 166 | PF00179 | 0.449 |
TRG_ENDOCYTIC_2 | 172 | 175 | PF00928 | 0.466 |
TRG_ENDOCYTIC_2 | 252 | 255 | PF00928 | 0.470 |
TRG_ENDOCYTIC_2 | 301 | 304 | PF00928 | 0.317 |
TRG_ENDOCYTIC_2 | 430 | 433 | PF00928 | 0.435 |
TRG_ENDOCYTIC_2 | 5 | 8 | PF00928 | 0.409 |
TRG_ER_diArg_1 | 149 | 152 | PF00400 | 0.356 |
TRG_ER_diArg_1 | 252 | 254 | PF00400 | 0.300 |
TRG_ER_diArg_1 | 339 | 341 | PF00400 | 0.711 |
TRG_ER_diArg_1 | 383 | 385 | PF00400 | 0.441 |
TRG_NES_CRM1_1 | 169 | 182 | PF08389 | 0.363 |
TRG_Pf-PMV_PEXEL_1 | 152 | 156 | PF00026 | 0.415 |
TRG_Pf-PMV_PEXEL_1 | 192 | 196 | PF00026 | 0.444 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HTJ1 | Leptomonas seymouri | 39% | 100% |
A0A0S4JLJ0 | Bodo saltans | 27% | 100% |
A0A1X0NWB3 | Trypanosomatidae | 25% | 100% |
A0A3Q8IF02 | Leishmania donovani | 73% | 100% |
A0A422NWV9 | Trypanosoma rangeli | 30% | 100% |
A4I0Z8 | Leishmania infantum | 73% | 100% |
C9ZWB1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
E9AX36 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 72% | 100% |
Q4QAE0 | Leishmania major | 72% | 100% |