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 | yes | yes: 1, no: 7 |
NetGPI | no | yes: 0, no: 8 |
Related structures:
AlphaFold database: A4HQ70
Term | Name | Level | Count |
---|---|---|---|
GO:0000049 | tRNA binding | 5 | 1 |
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003723 | RNA binding | 4 | 1 |
GO:0003824 | catalytic activity | 1 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0016301 | kinase activity | 4 | 1 |
GO:0016740 | transferase activity | 2 | 1 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 102 | 104 | PF00675 | 0.346 |
CLV_NRD_NRD_1 | 200 | 202 | PF00675 | 0.412 |
CLV_NRD_NRD_1 | 332 | 334 | PF00675 | 0.680 |
CLV_NRD_NRD_1 | 381 | 383 | PF00675 | 0.481 |
CLV_NRD_NRD_1 | 46 | 48 | PF00675 | 0.462 |
CLV_NRD_NRD_1 | 89 | 91 | PF00675 | 0.538 |
CLV_PCSK_FUR_1 | 330 | 334 | PF00082 | 0.702 |
CLV_PCSK_KEX2_1 | 102 | 104 | PF00082 | 0.486 |
CLV_PCSK_KEX2_1 | 200 | 202 | PF00082 | 0.429 |
CLV_PCSK_KEX2_1 | 330 | 332 | PF00082 | 0.650 |
CLV_PCSK_PC7_1 | 98 | 104 | PF00082 | 0.451 |
CLV_PCSK_SKI1_1 | 186 | 190 | PF00082 | 0.393 |
CLV_PCSK_SKI1_1 | 37 | 41 | PF00082 | 0.484 |
CLV_PCSK_SKI1_1 | 98 | 102 | PF00082 | 0.434 |
DEG_APCC_DBOX_1 | 396 | 404 | PF00400 | 0.351 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.607 |
DOC_CKS1_1 | 187 | 192 | PF01111 | 0.401 |
DOC_CKS1_1 | 372 | 377 | PF01111 | 0.361 |
DOC_CKS1_1 | 450 | 455 | PF01111 | 0.474 |
DOC_CYCLIN_RxL_1 | 434 | 444 | PF00134 | 0.281 |
DOC_CYCLIN_RxL_1 | 98 | 110 | PF00134 | 0.447 |
DOC_MAPK_DCC_7 | 125 | 135 | PF00069 | 0.380 |
DOC_MAPK_MEF2A_6 | 186 | 195 | PF00069 | 0.425 |
DOC_PP4_FxxP_1 | 187 | 190 | PF00568 | 0.447 |
DOC_SPAK_OSR1_1 | 395 | 399 | PF12202 | 0.326 |
DOC_USP7_MATH_1 | 169 | 173 | PF00917 | 0.685 |
DOC_USP7_MATH_1 | 213 | 217 | PF00917 | 0.589 |
DOC_USP7_MATH_1 | 26 | 30 | PF00917 | 0.393 |
DOC_WW_Pin1_4 | 161 | 166 | PF00397 | 0.566 |
DOC_WW_Pin1_4 | 186 | 191 | PF00397 | 0.385 |
DOC_WW_Pin1_4 | 371 | 376 | PF00397 | 0.603 |
DOC_WW_Pin1_4 | 4 | 9 | PF00397 | 0.743 |
DOC_WW_Pin1_4 | 449 | 454 | PF00397 | 0.461 |
DOC_WW_Pin1_4 | 90 | 95 | PF00397 | 0.454 |
LIG_14-3-3_CanoR_1 | 59 | 64 | PF00244 | 0.346 |
LIG_CSL_BTD_1 | 217 | 220 | PF09270 | 0.472 |
LIG_FHA_1 | 115 | 121 | PF00498 | 0.543 |
LIG_FHA_1 | 236 | 242 | PF00498 | 0.617 |
LIG_FHA_1 | 268 | 274 | PF00498 | 0.441 |
LIG_FHA_1 | 366 | 372 | PF00498 | 0.583 |
LIG_FHA_1 | 409 | 415 | PF00498 | 0.627 |
LIG_FHA_1 | 99 | 105 | PF00498 | 0.423 |
LIG_FHA_2 | 162 | 168 | PF00498 | 0.440 |
LIG_HCF-1_HBM_1 | 232 | 235 | PF13415 | 0.498 |
LIG_LIR_Apic_2 | 184 | 190 | PF02991 | 0.432 |
LIG_LIR_Apic_2 | 215 | 221 | PF02991 | 0.605 |
LIG_LIR_LC3C_4 | 428 | 431 | PF02991 | 0.266 |
LIG_LIR_Nem_3 | 260 | 266 | PF02991 | 0.454 |
LIG_LIR_Nem_3 | 276 | 282 | PF02991 | 0.646 |
LIG_LIR_Nem_3 | 289 | 293 | PF02991 | 0.304 |
LIG_LIR_Nem_3 | 89 | 95 | PF02991 | 0.373 |
LIG_NRBOX | 15 | 21 | PF00104 | 0.243 |
LIG_PCNA_PIPBox_1 | 435 | 444 | PF02747 | 0.338 |
LIG_PCNA_yPIPBox_3 | 435 | 443 | PF02747 | 0.331 |
LIG_PCNA_yPIPBox_3 | 55 | 64 | PF02747 | 0.420 |
LIG_Pex14_2 | 179 | 183 | PF04695 | 0.373 |
LIG_Rb_pABgroove_1 | 225 | 233 | PF01858 | 0.438 |
LIG_RPA_C_Fungi | 327 | 339 | PF08784 | 0.396 |
LIG_SH2_STAT3 | 160 | 163 | PF00017 | 0.530 |
LIG_SH3_1 | 2 | 8 | PF00018 | 0.512 |
LIG_SH3_1 | 80 | 86 | PF00018 | 0.455 |
LIG_SH3_3 | 2 | 8 | PF00018 | 0.765 |
LIG_SH3_3 | 216 | 222 | PF00018 | 0.507 |
LIG_SH3_3 | 80 | 86 | PF00018 | 0.550 |
LIG_SUMO_SIM_anti_2 | 14 | 21 | PF11976 | 0.248 |
LIG_SUMO_SIM_par_1 | 103 | 108 | PF11976 | 0.434 |
LIG_SUMO_SIM_par_1 | 131 | 137 | PF11976 | 0.265 |
LIG_SUMO_SIM_par_1 | 14 | 21 | PF11976 | 0.245 |
LIG_SUMO_SIM_par_1 | 411 | 417 | PF11976 | 0.569 |
LIG_SxIP_EBH_1 | 16 | 28 | PF03271 | 0.407 |
LIG_TRAF2_1 | 388 | 391 | PF00917 | 0.419 |
LIG_UBA3_1 | 19 | 28 | PF00899 | 0.263 |
MOD_CK1_1 | 168 | 174 | PF00069 | 0.655 |
MOD_CK1_1 | 370 | 376 | PF00069 | 0.446 |
MOD_CK1_1 | 7 | 13 | PF00069 | 0.590 |
MOD_CK2_1 | 140 | 146 | PF00069 | 0.476 |
MOD_GlcNHglycan | 109 | 112 | PF01048 | 0.478 |
MOD_GlcNHglycan | 13 | 16 | PF01048 | 0.442 |
MOD_GlcNHglycan | 171 | 174 | PF01048 | 0.514 |
MOD_GlcNHglycan | 215 | 218 | PF01048 | 0.512 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.518 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.590 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.640 |
MOD_GSK3_1 | 367 | 374 | PF00069 | 0.580 |
MOD_N-GLC_1 | 43 | 48 | PF02516 | 0.401 |
MOD_NEK2_1 | 105 | 110 | PF00069 | 0.492 |
MOD_NEK2_1 | 18 | 23 | PF00069 | 0.425 |
MOD_NEK2_1 | 381 | 386 | PF00069 | 0.326 |
MOD_PIKK_1 | 105 | 111 | PF00454 | 0.481 |
MOD_PIKK_1 | 257 | 263 | PF00454 | 0.516 |
MOD_PIKK_1 | 267 | 273 | PF00454 | 0.547 |
MOD_PIKK_1 | 355 | 361 | PF00454 | 0.301 |
MOD_PK_1 | 59 | 65 | PF00069 | 0.343 |
MOD_PKA_2 | 381 | 387 | PF00069 | 0.476 |
MOD_Plk_1 | 275 | 281 | PF00069 | 0.470 |
MOD_Plk_4 | 27 | 33 | PF00069 | 0.462 |
MOD_Plk_4 | 286 | 292 | PF00069 | 0.565 |
MOD_Plk_4 | 367 | 373 | PF00069 | 0.640 |
MOD_Plk_4 | 59 | 65 | PF00069 | 0.431 |
MOD_ProDKin_1 | 161 | 167 | PF00069 | 0.575 |
MOD_ProDKin_1 | 186 | 192 | PF00069 | 0.394 |
MOD_ProDKin_1 | 371 | 377 | PF00069 | 0.595 |
MOD_ProDKin_1 | 4 | 10 | PF00069 | 0.729 |
MOD_ProDKin_1 | 449 | 455 | PF00069 | 0.464 |
MOD_ProDKin_1 | 90 | 96 | PF00069 | 0.444 |
MOD_SUMO_for_1 | 388 | 391 | PF00179 | 0.523 |
TRG_DiLeu_BaLyEn_6 | 100 | 105 | PF01217 | 0.418 |
TRG_DiLeu_BaLyEn_6 | 91 | 96 | PF01217 | 0.432 |
TRG_ENDOCYTIC_2 | 141 | 144 | PF00928 | 0.374 |
TRG_ENDOCYTIC_2 | 148 | 151 | PF00928 | 0.344 |
TRG_ER_diArg_1 | 102 | 104 | PF00400 | 0.431 |
TRG_ER_diArg_1 | 330 | 333 | PF00400 | 0.675 |
TRG_Pf-PMV_PEXEL_1 | 102 | 106 | PF00026 | 0.451 |
TRG_Pf-PMV_PEXEL_1 | 153 | 158 | PF00026 | 0.372 |
TRG_Pf-PMV_PEXEL_1 | 401 | 406 | PF00026 | 0.394 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PFJ4 | Leptomonas seymouri | 36% | 98% |
A0A1X0P061 | Trypanosomatidae | 23% | 100% |
A0A3Q8ILN7 | Leishmania donovani | 73% | 100% |
A0A422NKD5 | Trypanosoma rangeli | 26% | 100% |
A4IDW8 | Leishmania infantum | 73% | 100% |
E9ATY9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 72% | 100% |
Q4Q0K7 | Leishmania major | 71% | 100% |