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: 12 |
NetGPI | no | yes: 0, no: 13 |
Related structures:
AlphaFold database: Q4Q5U9
Term | Name | Level | Count |
---|---|---|---|
GO:0009987 | cellular process | 1 | 2 |
GO:0016043 | cellular component organization | 3 | 2 |
GO:0022607 | cellular component assembly | 4 | 2 |
GO:0043933 | protein-containing complex organization | 4 | 2 |
GO:0051259 | protein complex oligomerization | 6 | 2 |
GO:0051260 | protein homooligomerization | 7 | 2 |
GO:0065003 | protein-containing complex assembly | 5 | 2 |
GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 153 | 157 | PF00656 | 0.649 |
CLV_C14_Caspase3-7 | 186 | 190 | PF00656 | 0.484 |
CLV_NRD_NRD_1 | 142 | 144 | PF00675 | 0.717 |
CLV_NRD_NRD_1 | 63 | 65 | PF00675 | 0.683 |
CLV_NRD_NRD_1 | 78 | 80 | PF00675 | 0.525 |
CLV_PCSK_KEX2_1 | 144 | 146 | PF00082 | 0.726 |
CLV_PCSK_KEX2_1 | 63 | 65 | PF00082 | 0.630 |
CLV_PCSK_KEX2_1 | 77 | 79 | PF00082 | 0.526 |
CLV_PCSK_PC1ET2_1 | 144 | 146 | PF00082 | 0.726 |
CLV_PCSK_PC1ET2_1 | 77 | 79 | PF00082 | 0.545 |
CLV_PCSK_SKI1_1 | 107 | 111 | PF00082 | 0.393 |
CLV_PCSK_SKI1_1 | 313 | 317 | PF00082 | 0.462 |
CLV_PCSK_SKI1_1 | 53 | 57 | PF00082 | 0.545 |
DOC_CKS1_1 | 271 | 276 | PF01111 | 0.542 |
DOC_CYCLIN_RxL_1 | 101 | 113 | PF00134 | 0.460 |
DOC_CYCLIN_RxL_1 | 50 | 58 | PF00134 | 0.544 |
DOC_CYCLIN_yCln2_LP_2 | 304 | 310 | PF00134 | 0.440 |
DOC_MAPK_gen_1 | 164 | 173 | PF00069 | 0.523 |
DOC_MAPK_MEF2A_6 | 167 | 175 | PF00069 | 0.407 |
DOC_PP1_RVXF_1 | 121 | 127 | PF00149 | 0.341 |
DOC_PP1_RVXF_1 | 287 | 293 | PF00149 | 0.412 |
DOC_PP1_RVXF_1 | 311 | 317 | PF00149 | 0.466 |
DOC_PP1_RVXF_1 | 319 | 326 | PF00149 | 0.483 |
DOC_PP4_FxxP_1 | 217 | 220 | PF00568 | 0.560 |
DOC_SPAK_OSR1_1 | 207 | 211 | PF12202 | 0.576 |
DOC_USP7_MATH_1 | 136 | 140 | PF00917 | 0.694 |
DOC_USP7_MATH_1 | 157 | 161 | PF00917 | 0.405 |
DOC_USP7_MATH_1 | 345 | 349 | PF00917 | 0.393 |
DOC_USP7_MATH_1 | 350 | 354 | PF00917 | 0.410 |
DOC_WW_Pin1_4 | 270 | 275 | PF00397 | 0.546 |
LIG_14-3-3_CanoR_1 | 207 | 217 | PF00244 | 0.563 |
LIG_14-3-3_CanoR_1 | 352 | 360 | PF00244 | 0.409 |
LIG_14-3-3_CanoR_1 | 44 | 54 | PF00244 | 0.688 |
LIG_BRCT_BRCA1_1 | 115 | 119 | PF00533 | 0.365 |
LIG_BRCT_BRCA1_1 | 235 | 239 | PF00533 | 0.430 |
LIG_FHA_1 | 153 | 159 | PF00498 | 0.617 |
LIG_FHA_2 | 151 | 157 | PF00498 | 0.640 |
LIG_LIR_Nem_3 | 194 | 200 | PF02991 | 0.346 |
LIG_MLH1_MIPbox_1 | 235 | 239 | PF16413 | 0.430 |
LIG_NRBOX | 171 | 177 | PF00104 | 0.375 |
LIG_PCNA_yPIPBox_3 | 164 | 172 | PF02747 | 0.407 |
LIG_Pex14_1 | 204 | 208 | PF04695 | 0.405 |
LIG_PTB_Apo_2 | 202 | 209 | PF02174 | 0.517 |
LIG_PTB_Apo_2 | 325 | 332 | PF02174 | 0.516 |
LIG_PTB_Phospho_1 | 325 | 331 | PF10480 | 0.515 |
LIG_SH2_GRB2like | 284 | 287 | PF00017 | 0.374 |
LIG_SH2_STAT5 | 216 | 219 | PF00017 | 0.570 |
LIG_SH2_STAT5 | 293 | 296 | PF00017 | 0.546 |
LIG_SH2_STAT5 | 331 | 334 | PF00017 | 0.519 |
LIG_SH3_3 | 156 | 162 | PF00018 | 0.540 |
LIG_SH3_3 | 268 | 274 | PF00018 | 0.545 |
LIG_SUMO_SIM_anti_2 | 10 | 15 | PF11976 | 0.447 |
LIG_SUMO_SIM_anti_2 | 353 | 361 | PF11976 | 0.531 |
LIG_SUMO_SIM_par_1 | 155 | 163 | PF11976 | 0.551 |
LIG_TRAF2_1 | 26 | 29 | PF00917 | 0.578 |
LIG_UBA3_1 | 171 | 180 | PF00899 | 0.424 |
MOD_CK1_1 | 128 | 134 | PF00069 | 0.609 |
MOD_CK1_1 | 150 | 156 | PF00069 | 0.461 |
MOD_CK1_1 | 354 | 360 | PF00069 | 0.536 |
MOD_CK1_1 | 49 | 55 | PF00069 | 0.713 |
MOD_CK2_1 | 157 | 163 | PF00069 | 0.588 |
MOD_CK2_1 | 187 | 193 | PF00069 | 0.458 |
MOD_CK2_1 | 23 | 29 | PF00069 | 0.538 |
MOD_CK2_1 | 65 | 71 | PF00069 | 0.585 |
MOD_Cter_Amidation | 141 | 144 | PF01082 | 0.581 |
MOD_GlcNHglycan | 130 | 133 | PF01048 | 0.535 |
MOD_GlcNHglycan | 138 | 141 | PF01048 | 0.585 |
MOD_GlcNHglycan | 200 | 203 | PF01048 | 0.564 |
MOD_GlcNHglycan | 266 | 269 | PF01048 | 0.529 |
MOD_GlcNHglycan | 57 | 60 | PF01048 | 0.710 |
MOD_GSK3_1 | 113 | 120 | PF00069 | 0.516 |
MOD_GSK3_1 | 143 | 150 | PF00069 | 0.672 |
MOD_GSK3_1 | 221 | 228 | PF00069 | 0.566 |
MOD_GSK3_1 | 233 | 240 | PF00069 | 0.364 |
MOD_GSK3_1 | 260 | 267 | PF00069 | 0.468 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.646 |
MOD_GSK3_1 | 350 | 357 | PF00069 | 0.523 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.545 |
MOD_LATS_1 | 141 | 147 | PF00433 | 0.728 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.517 |
MOD_NEK2_1 | 103 | 108 | PF00069 | 0.482 |
MOD_NEK2_1 | 117 | 122 | PF00069 | 0.295 |
MOD_NEK2_1 | 126 | 131 | PF00069 | 0.413 |
MOD_NEK2_1 | 203 | 208 | PF00069 | 0.488 |
MOD_NEK2_1 | 221 | 226 | PF00069 | 0.576 |
MOD_NEK2_1 | 238 | 243 | PF00069 | 0.324 |
MOD_NEK2_1 | 248 | 253 | PF00069 | 0.374 |
MOD_NEK2_1 | 260 | 265 | PF00069 | 0.464 |
MOD_NEK2_1 | 38 | 43 | PF00069 | 0.603 |
MOD_NEK2_1 | 55 | 60 | PF00069 | 0.629 |
MOD_NEK2_2 | 187 | 192 | PF00069 | 0.455 |
MOD_NEK2_2 | 288 | 293 | PF00069 | 0.475 |
MOD_PIKK_1 | 210 | 216 | PF00454 | 0.465 |
MOD_PIKK_1 | 248 | 254 | PF00454 | 0.434 |
MOD_PIKK_1 | 351 | 357 | PF00454 | 0.507 |
MOD_PIKK_1 | 85 | 91 | PF00454 | 0.287 |
MOD_PKA_1 | 143 | 149 | PF00069 | 0.712 |
MOD_PKA_1 | 63 | 69 | PF00069 | 0.467 |
MOD_PKA_2 | 351 | 357 | PF00069 | 0.429 |
MOD_PKA_2 | 63 | 69 | PF00069 | 0.610 |
MOD_PKB_1 | 145 | 153 | PF00069 | 0.528 |
MOD_Plk_1 | 150 | 156 | PF00069 | 0.528 |
MOD_Plk_1 | 246 | 252 | PF00069 | 0.504 |
MOD_Plk_2-3 | 65 | 71 | PF00069 | 0.622 |
MOD_Plk_4 | 113 | 119 | PF00069 | 0.369 |
MOD_Plk_4 | 288 | 294 | PF00069 | 0.480 |
MOD_Plk_4 | 354 | 360 | PF00069 | 0.512 |
MOD_Plk_4 | 46 | 52 | PF00069 | 0.693 |
MOD_Plk_4 | 7 | 13 | PF00069 | 0.469 |
MOD_ProDKin_1 | 270 | 276 | PF00069 | 0.545 |
TRG_DiLeu_BaLyEn_6 | 16 | 21 | PF01217 | 0.504 |
TRG_DiLeu_BaLyEn_6 | 51 | 56 | PF01217 | 0.680 |
TRG_ENDOCYTIC_2 | 80 | 83 | PF00928 | 0.564 |
TRG_ER_diArg_1 | 62 | 64 | PF00400 | 0.538 |
TRG_ER_diArg_1 | 78 | 80 | PF00400 | 0.432 |
TRG_NLS_MonoExtC_3 | 142 | 147 | PF00514 | 0.577 |
TRG_Pf-PMV_PEXEL_1 | 107 | 111 | PF00026 | 0.495 |
TRG_Pf-PMV_PEXEL_1 | 313 | 317 | PF00026 | 0.392 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3N2 | Leptomonas seymouri | 61% | 100% |
A0A1X0NIJ4 | Trypanosomatidae | 39% | 100% |
A0A3R7K9T3 | Trypanosoma rangeli | 36% | 100% |
A0A3S7X510 | Leishmania donovani | 95% | 100% |
A0A422P2R6 | Trypanosoma rangeli | 24% | 70% |
A4HJU7 | Leishmania braziliensis | 79% | 100% |
A4HJV2 | Leishmania braziliensis | 80% | 100% |
A4I7B4 | Leishmania infantum | 96% | 100% |
C9ZWJ3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 100% |
E9B2A7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
V5B9A8 | Trypanosoma cruzi | 37% | 100% |
V5DUU9 | Trypanosoma cruzi | 25% | 71% |