Proteases, Rhomboid-like
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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
Related structures:
AlphaFold database: A4HS82
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 10 |
GO:0004175 | endopeptidase activity | 4 | 10 |
GO:0004252 | serine-type endopeptidase activity | 5 | 10 |
GO:0008233 | peptidase activity | 3 | 10 |
GO:0008236 | serine-type peptidase activity | 4 | 10 |
GO:0016787 | hydrolase activity | 2 | 10 |
GO:0017171 | serine hydrolase activity | 3 | 10 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 164 | 168 | PF00656 | 0.656 |
CLV_NRD_NRD_1 | 73 | 75 | PF00675 | 0.397 |
CLV_PCSK_SKI1_1 | 18 | 22 | PF00082 | 0.405 |
CLV_PCSK_SKI1_1 | 357 | 361 | PF00082 | 0.252 |
CLV_PCSK_SKI1_1 | 46 | 50 | PF00082 | 0.584 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.614 |
DEG_SPOP_SBC_1 | 37 | 41 | PF00917 | 0.677 |
DEG_SPOP_SBC_1 | 66 | 70 | PF00917 | 0.639 |
DOC_CYCLIN_RxL_1 | 382 | 393 | PF00134 | 0.371 |
DOC_MAPK_gen_1 | 87 | 97 | PF00069 | 0.752 |
DOC_PP1_RVXF_1 | 329 | 336 | PF00149 | 0.290 |
DOC_PP4_FxxP_1 | 188 | 191 | PF00568 | 0.600 |
DOC_USP7_MATH_1 | 115 | 119 | PF00917 | 0.721 |
DOC_USP7_MATH_1 | 138 | 142 | PF00917 | 0.759 |
DOC_USP7_MATH_1 | 25 | 29 | PF00917 | 0.643 |
DOC_USP7_MATH_1 | 37 | 41 | PF00917 | 0.724 |
DOC_USP7_MATH_1 | 59 | 63 | PF00917 | 0.659 |
DOC_USP7_MATH_1 | 66 | 70 | PF00917 | 0.617 |
DOC_USP7_MATH_1 | 99 | 103 | PF00917 | 0.656 |
DOC_WW_Pin1_4 | 107 | 112 | PF00397 | 0.668 |
DOC_WW_Pin1_4 | 134 | 139 | PF00397 | 0.739 |
DOC_WW_Pin1_4 | 172 | 177 | PF00397 | 0.609 |
DOC_WW_Pin1_4 | 27 | 32 | PF00397 | 0.723 |
LIG_14-3-3_CanoR_1 | 100 | 104 | PF00244 | 0.633 |
LIG_14-3-3_CanoR_1 | 18 | 27 | PF00244 | 0.718 |
LIG_14-3-3_CanoR_1 | 275 | 279 | PF00244 | 0.315 |
LIG_14-3-3_CanoR_1 | 46 | 51 | PF00244 | 0.731 |
LIG_14-3-3_CanoR_1 | 74 | 83 | PF00244 | 0.740 |
LIG_BRCT_BRCA1_1 | 116 | 120 | PF00533 | 0.643 |
LIG_Clathr_ClatBox_1 | 322 | 326 | PF01394 | 0.290 |
LIG_deltaCOP1_diTrp_1 | 217 | 222 | PF00928 | 0.384 |
LIG_deltaCOP1_diTrp_1 | 232 | 241 | PF00928 | 0.271 |
LIG_deltaCOP1_diTrp_1 | 256 | 263 | PF00928 | 0.252 |
LIG_deltaCOP1_diTrp_1 | 354 | 359 | PF00928 | 0.290 |
LIG_EH_1 | 315 | 319 | PF12763 | 0.290 |
LIG_EVH1_1 | 186 | 190 | PF00568 | 0.606 |
LIG_EVH1_2 | 339 | 343 | PF00568 | 0.252 |
LIG_FHA_1 | 19 | 25 | PF00498 | 0.516 |
LIG_FHA_1 | 192 | 198 | PF00498 | 0.452 |
LIG_FHA_1 | 345 | 351 | PF00498 | 0.313 |
LIG_FHA_1 | 382 | 388 | PF00498 | 0.366 |
LIG_FHA_1 | 92 | 98 | PF00498 | 0.667 |
LIG_FHA_2 | 359 | 365 | PF00498 | 0.469 |
LIG_LIR_Gen_1 | 232 | 241 | PF02991 | 0.334 |
LIG_LIR_Gen_1 | 277 | 285 | PF02991 | 0.315 |
LIG_LIR_Gen_1 | 347 | 355 | PF02991 | 0.290 |
LIG_LIR_Nem_3 | 217 | 222 | PF02991 | 0.375 |
LIG_LIR_Nem_3 | 232 | 237 | PF02991 | 0.280 |
LIG_LIR_Nem_3 | 277 | 282 | PF02991 | 0.315 |
LIG_LIR_Nem_3 | 347 | 352 | PF02991 | 0.290 |
LIG_LIR_Nem_3 | 354 | 359 | PF02991 | 0.290 |
LIG_LYPXL_S_1 | 237 | 241 | PF13949 | 0.452 |
LIG_Pex14_1 | 234 | 238 | PF04695 | 0.334 |
LIG_Pex14_2 | 188 | 192 | PF04695 | 0.599 |
LIG_Pex14_2 | 241 | 245 | PF04695 | 0.294 |
LIG_PTB_Apo_2 | 240 | 247 | PF02174 | 0.269 |
LIG_PTB_Phospho_1 | 240 | 246 | PF10480 | 0.269 |
LIG_REV1ctd_RIR_1 | 4 | 14 | PF16727 | 0.591 |
LIG_SH2_STAT5 | 185 | 188 | PF00017 | 0.610 |
LIG_SH2_STAT5 | 209 | 212 | PF00017 | 0.292 |
LIG_SH2_STAT5 | 377 | 380 | PF00017 | 0.290 |
LIG_SH3_3 | 184 | 190 | PF00018 | 0.610 |
LIG_SH3_3 | 336 | 342 | PF00018 | 0.267 |
LIG_SUMO_SIM_par_1 | 321 | 326 | PF11976 | 0.350 |
LIG_UBA3_1 | 386 | 391 | PF00899 | 0.373 |
MOD_CDC14_SPxK_1 | 137 | 140 | PF00782 | 0.731 |
MOD_CDK_SPK_2 | 134 | 139 | PF00069 | 0.739 |
MOD_CDK_SPxK_1 | 134 | 140 | PF00069 | 0.727 |
MOD_CK1_1 | 39 | 45 | PF00069 | 0.725 |
MOD_CK1_1 | 69 | 75 | PF00069 | 0.717 |
MOD_CK2_1 | 166 | 172 | PF00069 | 0.631 |
MOD_CK2_1 | 358 | 364 | PF00069 | 0.469 |
MOD_CMANNOS | 258 | 261 | PF00535 | 0.452 |
MOD_GlcNHglycan | 167 | 171 | PF01048 | 0.533 |
MOD_GlcNHglycan | 180 | 183 | PF01048 | 0.464 |
MOD_GlcNHglycan | 52 | 55 | PF01048 | 0.485 |
MOD_GlcNHglycan | 61 | 64 | PF01048 | 0.459 |
MOD_GlcNHglycan | 76 | 79 | PF01048 | 0.534 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.735 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.766 |
MOD_GSK3_1 | 14 | 21 | PF00069 | 0.630 |
MOD_GSK3_1 | 281 | 288 | PF00069 | 0.298 |
MOD_GSK3_1 | 36 | 43 | PF00069 | 0.651 |
MOD_GSK3_1 | 46 | 53 | PF00069 | 0.769 |
MOD_GSK3_1 | 61 | 68 | PF00069 | 0.595 |
MOD_GSK3_1 | 74 | 81 | PF00069 | 0.703 |
MOD_N-GLC_1 | 232 | 237 | PF02516 | 0.598 |
MOD_NEK2_1 | 263 | 268 | PF00069 | 0.252 |
MOD_NEK2_1 | 271 | 276 | PF00069 | 0.252 |
MOD_NEK2_1 | 281 | 286 | PF00069 | 0.290 |
MOD_NEK2_1 | 344 | 349 | PF00069 | 0.290 |
MOD_NEK2_1 | 38 | 43 | PF00069 | 0.695 |
MOD_NEK2_2 | 115 | 120 | PF00069 | 0.645 |
MOD_NEK2_2 | 85 | 90 | PF00069 | 0.756 |
MOD_NEK2_2 | 99 | 104 | PF00069 | 0.637 |
MOD_PIKK_1 | 69 | 75 | PF00454 | 0.641 |
MOD_PKA_1 | 139 | 145 | PF00069 | 0.668 |
MOD_PKA_1 | 74 | 80 | PF00069 | 0.601 |
MOD_PKA_2 | 129 | 135 | PF00069 | 0.732 |
MOD_PKA_2 | 14 | 20 | PF00069 | 0.694 |
MOD_PKA_2 | 25 | 31 | PF00069 | 0.731 |
MOD_PKA_2 | 274 | 280 | PF00069 | 0.315 |
MOD_PKA_2 | 99 | 105 | PF00069 | 0.633 |
MOD_Plk_1 | 232 | 238 | PF00069 | 0.397 |
MOD_Plk_4 | 115 | 121 | PF00069 | 0.760 |
MOD_Plk_4 | 263 | 269 | PF00069 | 0.269 |
MOD_Plk_4 | 274 | 280 | PF00069 | 0.290 |
MOD_Plk_4 | 285 | 291 | PF00069 | 0.269 |
MOD_Plk_4 | 91 | 97 | PF00069 | 0.660 |
MOD_Plk_4 | 99 | 105 | PF00069 | 0.615 |
MOD_ProDKin_1 | 107 | 113 | PF00069 | 0.662 |
MOD_ProDKin_1 | 134 | 140 | PF00069 | 0.741 |
MOD_ProDKin_1 | 172 | 178 | PF00069 | 0.606 |
MOD_ProDKin_1 | 27 | 33 | PF00069 | 0.726 |
TRG_DiLeu_BaLyEn_6 | 43 | 48 | PF01217 | 0.596 |
TRG_ENDOCYTIC_2 | 185 | 188 | PF00928 | 0.610 |
TRG_ENDOCYTIC_2 | 209 | 212 | PF00928 | 0.290 |
TRG_ENDOCYTIC_2 | 238 | 241 | PF00928 | 0.252 |
TRG_ENDOCYTIC_2 | 300 | 303 | PF00928 | 0.469 |
TRG_ER_diArg_1 | 308 | 311 | PF00400 | 0.452 |
TRG_Pf-PMV_PEXEL_1 | 385 | 390 | PF00026 | 0.573 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PA30 | Leptomonas seymouri | 81% | 100% |
A0A1X0NLI4 | Trypanosomatidae | 64% | 100% |
A0A3R7RFZ5 | Trypanosoma rangeli | 63% | 100% |
A0A3S7WNU2 | Leishmania donovani | 100% | 100% |
A4H3Z5 | Leishmania braziliensis | 92% | 100% |
C9ZY76 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 65% | 100% |
E9AK68 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 98% |
Q9U0Z8 | Leishmania major | 96% | 100% |