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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 16 |
NetGPI | no | yes: 0, no: 16 |
Term | Name | Level | Count |
---|---|---|---|
GO:0051286 | cell tip | 3 | 1 |
GO:0060187 | cell pole | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: Q4Q3I8
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 1 |
GO:0016740 | transferase activity | 2 | 1 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 1 |
GO:0016779 | nucleotidyltransferase activity | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 384 | 388 | PF00656 | 0.734 |
CLV_NRD_NRD_1 | 133 | 135 | PF00675 | 0.366 |
CLV_NRD_NRD_1 | 442 | 444 | PF00675 | 0.383 |
CLV_PCSK_KEX2_1 | 133 | 135 | PF00082 | 0.366 |
CLV_PCSK_KEX2_1 | 442 | 444 | PF00082 | 0.382 |
CLV_PCSK_SKI1_1 | 144 | 148 | PF00082 | 0.322 |
CLV_PCSK_SKI1_1 | 270 | 274 | PF00082 | 0.349 |
CLV_PCSK_SKI1_1 | 31 | 35 | PF00082 | 0.388 |
CLV_PCSK_SKI1_1 | 423 | 427 | PF00082 | 0.296 |
CLV_PCSK_SKI1_1 | 443 | 447 | PF00082 | 0.363 |
CLV_PCSK_SKI1_1 | 59 | 63 | PF00082 | 0.378 |
DEG_APCC_DBOX_1 | 30 | 38 | PF00400 | 0.401 |
DEG_SCF_FBW7_1 | 365 | 371 | PF00400 | 0.583 |
DEG_SCF_FBW7_2 | 241 | 247 | PF00400 | 0.514 |
DOC_CDC14_PxL_1 | 341 | 349 | PF14671 | 0.288 |
DOC_CKS1_1 | 241 | 246 | PF01111 | 0.492 |
DOC_CKS1_1 | 365 | 370 | PF01111 | 0.786 |
DOC_CYCLIN_yCln2_LP_2 | 246 | 252 | PF00134 | 0.384 |
DOC_CYCLIN_yCln2_LP_2 | 4 | 7 | PF00134 | 0.350 |
DOC_MAPK_gen_1 | 144 | 154 | PF00069 | 0.281 |
DOC_MAPK_MEF2A_6 | 171 | 179 | PF00069 | 0.285 |
DOC_MAPK_MEF2A_6 | 315 | 322 | PF00069 | 0.381 |
DOC_PP1_RVXF_1 | 124 | 131 | PF00149 | 0.463 |
DOC_PP1_RVXF_1 | 29 | 36 | PF00149 | 0.288 |
DOC_PP1_RVXF_1 | 456 | 462 | PF00149 | 0.361 |
DOC_PP2B_LxvP_1 | 195 | 198 | PF13499 | 0.475 |
DOC_PP2B_LxvP_1 | 212 | 215 | PF13499 | 0.252 |
DOC_PP2B_LxvP_1 | 396 | 399 | PF13499 | 0.490 |
DOC_PP2B_LxvP_1 | 4 | 7 | PF13499 | 0.350 |
DOC_USP7_MATH_1 | 309 | 313 | PF00917 | 0.401 |
DOC_USP7_MATH_1 | 374 | 378 | PF00917 | 0.708 |
DOC_WW_Pin1_4 | 240 | 245 | PF00397 | 0.520 |
DOC_WW_Pin1_4 | 253 | 258 | PF00397 | 0.259 |
DOC_WW_Pin1_4 | 294 | 299 | PF00397 | 0.294 |
DOC_WW_Pin1_4 | 347 | 352 | PF00397 | 0.356 |
DOC_WW_Pin1_4 | 358 | 363 | PF00397 | 0.600 |
DOC_WW_Pin1_4 | 364 | 369 | PF00397 | 0.759 |
DOC_WW_Pin1_4 | 370 | 375 | PF00397 | 0.682 |
DOC_WW_Pin1_4 | 459 | 464 | PF00397 | 0.398 |
LIG_14-3-3_CanoR_1 | 307 | 316 | PF00244 | 0.474 |
LIG_BRCT_BRCA1_1 | 177 | 181 | PF00533 | 0.366 |
LIG_Clathr_ClatBox_1 | 37 | 41 | PF01394 | 0.288 |
LIG_FHA_1 | 123 | 129 | PF00498 | 0.543 |
LIG_FHA_1 | 168 | 174 | PF00498 | 0.365 |
LIG_FHA_1 | 208 | 214 | PF00498 | 0.378 |
LIG_FHA_1 | 226 | 232 | PF00498 | 0.194 |
LIG_FHA_1 | 241 | 247 | PF00498 | 0.570 |
LIG_FHA_1 | 309 | 315 | PF00498 | 0.402 |
LIG_FHA_1 | 448 | 454 | PF00498 | 0.345 |
LIG_FHA_1 | 506 | 512 | PF00498 | 0.348 |
LIG_FHA_1 | 87 | 93 | PF00498 | 0.365 |
LIG_FHA_2 | 200 | 206 | PF00498 | 0.431 |
LIG_FHA_2 | 370 | 376 | PF00498 | 0.726 |
LIG_LIR_Apic_2 | 131 | 135 | PF02991 | 0.498 |
LIG_LIR_Gen_1 | 206 | 215 | PF02991 | 0.431 |
LIG_LIR_Nem_3 | 140 | 146 | PF02991 | 0.327 |
LIG_LIR_Nem_3 | 206 | 212 | PF02991 | 0.431 |
LIG_LIR_Nem_3 | 23 | 28 | PF02991 | 0.333 |
LIG_LIR_Nem_3 | 266 | 272 | PF02991 | 0.265 |
LIG_LIR_Nem_3 | 289 | 294 | PF02991 | 0.288 |
LIG_LIR_Nem_3 | 32 | 38 | PF02991 | 0.301 |
LIG_LIR_Nem_3 | 419 | 425 | PF02991 | 0.336 |
LIG_PCNA_yPIPBox_3 | 144 | 157 | PF02747 | 0.301 |
LIG_PCNA_yPIPBox_3 | 270 | 284 | PF02747 | 0.415 |
LIG_PCNA_yPIPBox_3 | 423 | 437 | PF02747 | 0.285 |
LIG_Pex14_2 | 102 | 106 | PF04695 | 0.373 |
LIG_Pex14_2 | 114 | 118 | PF04695 | 0.294 |
LIG_Pex14_2 | 506 | 510 | PF04695 | 0.344 |
LIG_SH2_CRK | 132 | 136 | PF00017 | 0.323 |
LIG_SH2_CRK | 139 | 143 | PF00017 | 0.305 |
LIG_SH2_CRK | 209 | 213 | PF00017 | 0.401 |
LIG_SH2_NCK_1 | 139 | 143 | PF00017 | 0.344 |
LIG_SH2_NCK_1 | 354 | 358 | PF00017 | 0.380 |
LIG_SH2_SRC | 252 | 255 | PF00017 | 0.527 |
LIG_SH2_STAP1 | 139 | 143 | PF00017 | 0.324 |
LIG_SH2_STAP1 | 209 | 213 | PF00017 | 0.288 |
LIG_SH2_STAP1 | 229 | 233 | PF00017 | 0.162 |
LIG_SH2_STAP1 | 354 | 358 | PF00017 | 0.401 |
LIG_SH2_STAT5 | 209 | 212 | PF00017 | 0.457 |
LIG_SH2_STAT5 | 229 | 232 | PF00017 | 0.162 |
LIG_SH2_STAT5 | 252 | 255 | PF00017 | 0.552 |
LIG_SH2_STAT5 | 300 | 303 | PF00017 | 0.401 |
LIG_SH2_STAT5 | 405 | 408 | PF00017 | 0.597 |
LIG_SH3_1 | 132 | 138 | PF00018 | 0.244 |
LIG_SH3_3 | 132 | 138 | PF00018 | 0.244 |
LIG_SH3_3 | 235 | 241 | PF00018 | 0.500 |
LIG_SH3_3 | 345 | 351 | PF00018 | 0.402 |
LIG_SH3_3 | 359 | 365 | PF00018 | 0.596 |
LIG_SH3_3 | 373 | 379 | PF00018 | 0.627 |
LIG_SH3_3 | 391 | 397 | PF00018 | 0.548 |
LIG_SH3_3 | 58 | 64 | PF00018 | 0.399 |
LIG_SUMO_SIM_anti_2 | 258 | 263 | PF11976 | 0.259 |
LIG_SUMO_SIM_anti_2 | 411 | 416 | PF11976 | 0.402 |
LIG_SUMO_SIM_anti_2 | 449 | 458 | PF11976 | 0.288 |
LIG_TRAF2_2 | 379 | 384 | PF00917 | 0.529 |
LIG_TRAF2_2 | 70 | 75 | PF00917 | 0.274 |
LIG_TYR_ITIM | 137 | 142 | PF00017 | 0.344 |
LIG_TYR_ITIM | 207 | 212 | PF00017 | 0.288 |
LIG_UBA3_1 | 33 | 42 | PF00899 | 0.308 |
MOD_CK1_1 | 369 | 375 | PF00069 | 0.707 |
MOD_CK2_1 | 102 | 108 | PF00069 | 0.398 |
MOD_CK2_1 | 199 | 205 | PF00069 | 0.456 |
MOD_CK2_1 | 323 | 329 | PF00069 | 0.391 |
MOD_CK2_1 | 369 | 375 | PF00069 | 0.735 |
MOD_GlcNHglycan | 183 | 186 | PF01048 | 0.426 |
MOD_GlcNHglycan | 407 | 410 | PF01048 | 0.454 |
MOD_GlcNHglycan | 480 | 483 | PF01048 | 0.267 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.324 |
MOD_GSK3_1 | 199 | 206 | PF00069 | 0.389 |
MOD_GSK3_1 | 364 | 371 | PF00069 | 0.672 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.380 |
MOD_N-GLC_1 | 167 | 172 | PF02516 | 0.324 |
MOD_N-GLC_1 | 294 | 299 | PF02516 | 0.309 |
MOD_N-GLC_1 | 447 | 452 | PF02516 | 0.324 |
MOD_N-GLC_1 | 48 | 53 | PF02516 | 0.306 |
MOD_NEK2_1 | 102 | 107 | PF00069 | 0.470 |
MOD_NEK2_1 | 175 | 180 | PF00069 | 0.383 |
MOD_NEK2_1 | 190 | 195 | PF00069 | 0.255 |
MOD_NEK2_1 | 470 | 475 | PF00069 | 0.338 |
MOD_Plk_1 | 410 | 416 | PF00069 | 0.501 |
MOD_Plk_1 | 92 | 98 | PF00069 | 0.291 |
MOD_Plk_2-3 | 88 | 94 | PF00069 | 0.401 |
MOD_Plk_4 | 102 | 108 | PF00069 | 0.354 |
MOD_Plk_4 | 203 | 209 | PF00069 | 0.384 |
MOD_Plk_4 | 286 | 292 | PF00069 | 0.288 |
MOD_Plk_4 | 410 | 416 | PF00069 | 0.490 |
MOD_Plk_4 | 470 | 476 | PF00069 | 0.288 |
MOD_Plk_4 | 480 | 486 | PF00069 | 0.418 |
MOD_Plk_4 | 63 | 69 | PF00069 | 0.413 |
MOD_ProDKin_1 | 240 | 246 | PF00069 | 0.521 |
MOD_ProDKin_1 | 253 | 259 | PF00069 | 0.259 |
MOD_ProDKin_1 | 294 | 300 | PF00069 | 0.294 |
MOD_ProDKin_1 | 347 | 353 | PF00069 | 0.356 |
MOD_ProDKin_1 | 358 | 364 | PF00069 | 0.608 |
MOD_ProDKin_1 | 366 | 372 | PF00069 | 0.525 |
MOD_ProDKin_1 | 375 | 381 | PF00069 | 0.562 |
MOD_ProDKin_1 | 459 | 465 | PF00069 | 0.398 |
MOD_SUMO_rev_2 | 104 | 114 | PF00179 | 0.412 |
TRG_DiLeu_BaEn_2 | 493 | 499 | PF01217 | 0.435 |
TRG_ENDOCYTIC_2 | 139 | 142 | PF00928 | 0.315 |
TRG_ENDOCYTIC_2 | 143 | 146 | PF00928 | 0.317 |
TRG_ENDOCYTIC_2 | 209 | 212 | PF00928 | 0.401 |
TRG_ENDOCYTIC_2 | 25 | 28 | PF00928 | 0.356 |
TRG_ENDOCYTIC_2 | 422 | 425 | PF00928 | 0.349 |
TRG_ER_diArg_1 | 132 | 134 | PF00400 | 0.550 |
TRG_ER_diArg_1 | 442 | 444 | PF00400 | 0.324 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I505 | Leptomonas seymouri | 64% | 96% |
A0A0N1PDX2 | Leptomonas seymouri | 38% | 100% |
A0A1X0P8U8 | Trypanosomatidae | 41% | 100% |
A0A3Q8IE32 | Leishmania donovani | 96% | 100% |
A0A3S7X7C8 | Leishmania donovani | 40% | 100% |
A4HAD7 | Leishmania braziliensis | 40% | 100% |
A4HAD8 | Leishmania braziliensis | 81% | 100% |
A4I9I9 | Leishmania infantum | 40% | 100% |
A4I9J0 | Leishmania infantum | 96% | 100% |
C9ZT01 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
D0A1U7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
E9B4I7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 39% | 100% |
E9B4I8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
Q4Q3I9 | Leishmania major | 40% | 100% |
V5B262 | Trypanosoma cruzi | 38% | 100% |