Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 2 |
Forrest at al. (procyclic) | no | yes: 2 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 3 |
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: 36 |
NetGPI | no | yes: 0, no: 36 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: Q4QE87
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 34 |
GO:0016787 | hydrolase activity | 2 | 34 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 404 | 406 | PF00675 | 0.520 |
CLV_PCSK_KEX2_1 | 237 | 239 | PF00082 | 0.305 |
CLV_PCSK_KEX2_1 | 276 | 278 | PF00082 | 0.257 |
CLV_PCSK_PC1ET2_1 | 237 | 239 | PF00082 | 0.409 |
CLV_PCSK_PC1ET2_1 | 276 | 278 | PF00082 | 0.294 |
CLV_PCSK_SKI1_1 | 234 | 238 | PF00082 | 0.309 |
CLV_PCSK_SKI1_1 | 269 | 273 | PF00082 | 0.309 |
CLV_PCSK_SKI1_1 | 286 | 290 | PF00082 | 0.237 |
CLV_PCSK_SKI1_1 | 325 | 329 | PF00082 | 0.193 |
DEG_APCC_DBOX_1 | 21 | 29 | PF00400 | 0.264 |
DEG_APCC_DBOX_1 | 285 | 293 | PF00400 | 0.403 |
DEG_SPOP_SBC_1 | 207 | 211 | PF00917 | 0.334 |
DOC_CKS1_1 | 331 | 336 | PF01111 | 0.342 |
DOC_CYCLIN_RxL_1 | 172 | 183 | PF00134 | 0.261 |
DOC_MAPK_DCC_7 | 332 | 342 | PF00069 | 0.325 |
DOC_MAPK_gen_1 | 273 | 281 | PF00069 | 0.372 |
DOC_MAPK_MEF2A_6 | 49 | 57 | PF00069 | 0.289 |
DOC_MIT_MIM_1 | 146 | 155 | PF04212 | 0.193 |
DOC_PP1_RVXF_1 | 147 | 153 | PF00149 | 0.193 |
DOC_PP2B_LxvP_1 | 10 | 13 | PF13499 | 0.716 |
DOC_PP2B_LxvP_1 | 292 | 295 | PF13499 | 0.361 |
DOC_PP2B_PxIxI_1 | 337 | 343 | PF00149 | 0.214 |
DOC_PP4_FxxP_1 | 335 | 338 | PF00568 | 0.193 |
DOC_USP7_MATH_1 | 241 | 245 | PF00917 | 0.298 |
DOC_USP7_MATH_1 | 399 | 403 | PF00917 | 0.430 |
DOC_USP7_MATH_1 | 5 | 9 | PF00917 | 0.773 |
DOC_USP7_UBL2_3 | 423 | 427 | PF12436 | 0.702 |
DOC_WW_Pin1_4 | 185 | 190 | PF00397 | 0.334 |
DOC_WW_Pin1_4 | 330 | 335 | PF00397 | 0.256 |
DOC_WW_Pin1_4 | 58 | 63 | PF00397 | 0.292 |
DOC_WW_Pin1_4 | 8 | 13 | PF00397 | 0.615 |
LIG_14-3-3_CanoR_1 | 175 | 180 | PF00244 | 0.294 |
LIG_14-3-3_CanoR_1 | 238 | 246 | PF00244 | 0.335 |
LIG_14-3-3_CanoR_1 | 30 | 38 | PF00244 | 0.434 |
LIG_14-3-3_CanoR_1 | 302 | 311 | PF00244 | 0.344 |
LIG_14-3-3_CanoR_1 | 325 | 335 | PF00244 | 0.460 |
LIG_14-3-3_CanoR_1 | 356 | 362 | PF00244 | 0.332 |
LIG_14-3-3_CanoR_1 | 69 | 74 | PF00244 | 0.416 |
LIG_Actin_WH2_1 | 366 | 384 | PF00022 | 0.394 |
LIG_BIR_III_4 | 140 | 144 | PF00653 | 0.406 |
LIG_FHA_1 | 109 | 115 | PF00498 | 0.469 |
LIG_FHA_1 | 14 | 20 | PF00498 | 0.480 |
LIG_FHA_1 | 326 | 332 | PF00498 | 0.297 |
LIG_FHA_1 | 337 | 343 | PF00498 | 0.250 |
LIG_FHA_1 | 35 | 41 | PF00498 | 0.379 |
LIG_FHA_2 | 131 | 137 | PF00498 | 0.303 |
LIG_FHA_2 | 220 | 226 | PF00498 | 0.193 |
LIG_FHA_2 | 92 | 98 | PF00498 | 0.337 |
LIG_LIR_Apic_2 | 333 | 338 | PF02991 | 0.191 |
LIG_LIR_Gen_1 | 201 | 207 | PF02991 | 0.392 |
LIG_LIR_Gen_1 | 244 | 253 | PF02991 | 0.411 |
LIG_LIR_Gen_1 | 383 | 393 | PF02991 | 0.368 |
LIG_LIR_Gen_1 | 77 | 85 | PF02991 | 0.423 |
LIG_LIR_Nem_3 | 111 | 116 | PF02991 | 0.333 |
LIG_LIR_Nem_3 | 140 | 145 | PF02991 | 0.397 |
LIG_LIR_Nem_3 | 201 | 205 | PF02991 | 0.345 |
LIG_LIR_Nem_3 | 244 | 249 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 383 | 388 | PF02991 | 0.392 |
LIG_LIR_Nem_3 | 77 | 83 | PF02991 | 0.313 |
LIG_NRBOX | 69 | 75 | PF00104 | 0.262 |
LIG_PDZ_Class_1 | 427 | 432 | PF00595 | 0.682 |
LIG_SH2_CRK | 80 | 84 | PF00017 | 0.472 |
LIG_SH2_GRB2like | 116 | 119 | PF00017 | 0.152 |
LIG_SH2_NCK_1 | 116 | 120 | PF00017 | 0.152 |
LIG_SH2_PTP2 | 385 | 388 | PF00017 | 0.451 |
LIG_SH2_SRC | 116 | 119 | PF00017 | 0.214 |
LIG_SH2_STAP1 | 116 | 120 | PF00017 | 0.415 |
LIG_SH2_STAP1 | 214 | 218 | PF00017 | 0.408 |
LIG_SH2_STAP1 | 242 | 246 | PF00017 | 0.410 |
LIG_SH2_STAT5 | 113 | 116 | PF00017 | 0.410 |
LIG_SH2_STAT5 | 132 | 135 | PF00017 | 0.313 |
LIG_SH2_STAT5 | 336 | 339 | PF00017 | 0.390 |
LIG_SH2_STAT5 | 368 | 371 | PF00017 | 0.336 |
LIG_SH2_STAT5 | 385 | 388 | PF00017 | 0.396 |
LIG_SH3_3 | 1 | 7 | PF00018 | 0.734 |
LIG_SH3_3 | 104 | 110 | PF00018 | 0.439 |
LIG_SH3_3 | 15 | 21 | PF00018 | 0.631 |
LIG_SH3_3 | 345 | 351 | PF00018 | 0.288 |
LIG_SUMO_SIM_anti_2 | 178 | 184 | PF11976 | 0.235 |
LIG_SUMO_SIM_par_1 | 174 | 180 | PF11976 | 0.278 |
LIG_TRAF2_1 | 223 | 226 | PF00917 | 0.410 |
LIG_UBA3_1 | 199 | 208 | PF00899 | 0.366 |
LIG_WRC_WIRS_1 | 199 | 204 | PF05994 | 0.285 |
LIG_WRC_WIRS_1 | 42 | 47 | PF05994 | 0.320 |
MOD_CDK_SPxxK_3 | 8 | 15 | PF00069 | 0.682 |
MOD_CK1_1 | 183 | 189 | PF00069 | 0.289 |
MOD_CK1_1 | 201 | 207 | PF00069 | 0.219 |
MOD_CK1_1 | 407 | 413 | PF00069 | 0.676 |
MOD_CK1_1 | 8 | 14 | PF00069 | 0.712 |
MOD_CK2_1 | 124 | 130 | PF00069 | 0.344 |
MOD_CK2_1 | 219 | 225 | PF00069 | 0.314 |
MOD_Cter_Amidation | 403 | 406 | PF01082 | 0.414 |
MOD_GlcNHglycan | 210 | 213 | PF01048 | 0.390 |
MOD_GlcNHglycan | 222 | 225 | PF01048 | 0.409 |
MOD_GlcNHglycan | 253 | 256 | PF01048 | 0.364 |
MOD_GlcNHglycan | 328 | 331 | PF01048 | 0.414 |
MOD_GlcNHglycan | 76 | 79 | PF01048 | 0.455 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.269 |
MOD_GSK3_1 | 237 | 244 | PF00069 | 0.327 |
MOD_GSK3_1 | 251 | 258 | PF00069 | 0.329 |
MOD_GSK3_1 | 275 | 282 | PF00069 | 0.227 |
MOD_GSK3_1 | 30 | 37 | PF00069 | 0.507 |
MOD_GSK3_1 | 321 | 328 | PF00069 | 0.423 |
MOD_GSK3_1 | 404 | 411 | PF00069 | 0.590 |
MOD_N-GLC_1 | 321 | 326 | PF02516 | 0.218 |
MOD_NEK2_1 | 155 | 160 | PF00069 | 0.343 |
MOD_NEK2_1 | 177 | 182 | PF00069 | 0.293 |
MOD_NEK2_1 | 275 | 280 | PF00069 | 0.284 |
MOD_NEK2_1 | 311 | 316 | PF00069 | 0.228 |
MOD_NEK2_1 | 373 | 378 | PF00069 | 0.361 |
MOD_NEK2_1 | 381 | 386 | PF00069 | 0.393 |
MOD_NEK2_1 | 74 | 79 | PF00069 | 0.410 |
MOD_NEK2_2 | 124 | 129 | PF00069 | 0.214 |
MOD_PIKK_1 | 309 | 315 | PF00454 | 0.450 |
MOD_PIKK_1 | 404 | 410 | PF00454 | 0.359 |
MOD_PK_1 | 304 | 310 | PF00069 | 0.415 |
MOD_PKA_1 | 237 | 243 | PF00069 | 0.152 |
MOD_PKA_2 | 219 | 225 | PF00069 | 0.193 |
MOD_PKA_2 | 237 | 243 | PF00069 | 0.428 |
MOD_PKA_2 | 251 | 257 | PF00069 | 0.224 |
MOD_PKA_2 | 303 | 309 | PF00069 | 0.405 |
MOD_PKA_2 | 381 | 387 | PF00069 | 0.473 |
MOD_PKA_2 | 404 | 410 | PF00069 | 0.519 |
MOD_PKB_1 | 302 | 310 | PF00069 | 0.214 |
MOD_Plk_2-3 | 130 | 136 | PF00069 | 0.286 |
MOD_Plk_4 | 109 | 115 | PF00069 | 0.355 |
MOD_Plk_4 | 177 | 183 | PF00069 | 0.253 |
MOD_Plk_4 | 198 | 204 | PF00069 | 0.359 |
MOD_Plk_4 | 336 | 342 | PF00069 | 0.269 |
MOD_Plk_4 | 357 | 363 | PF00069 | 0.297 |
MOD_Plk_4 | 373 | 379 | PF00069 | 0.278 |
MOD_Plk_4 | 381 | 387 | PF00069 | 0.426 |
MOD_Plk_4 | 69 | 75 | PF00069 | 0.412 |
MOD_ProDKin_1 | 185 | 191 | PF00069 | 0.334 |
MOD_ProDKin_1 | 330 | 336 | PF00069 | 0.256 |
MOD_ProDKin_1 | 58 | 64 | PF00069 | 0.292 |
MOD_ProDKin_1 | 8 | 14 | PF00069 | 0.614 |
MOD_SUMO_rev_2 | 233 | 239 | PF00179 | 0.277 |
TRG_AP2beta_CARGO_1 | 140 | 149 | PF09066 | 0.193 |
TRG_DiLeu_BaEn_4 | 225 | 231 | PF01217 | 0.410 |
TRG_ENDOCYTIC_2 | 385 | 388 | PF00928 | 0.463 |
TRG_ENDOCYTIC_2 | 42 | 45 | PF00928 | 0.332 |
TRG_ENDOCYTIC_2 | 80 | 83 | PF00928 | 0.331 |
TRG_ER_diArg_1 | 148 | 151 | PF00400 | 0.414 |
TRG_ER_diArg_1 | 19 | 22 | PF00400 | 0.582 |
TRG_ER_diArg_1 | 227 | 230 | PF00400 | 0.383 |
TRG_ER_diArg_1 | 301 | 304 | PF00400 | 0.375 |
TRG_Pf-PMV_PEXEL_1 | 126 | 130 | PF00026 | 0.345 |
TRG_PTS1 | 429 | 432 | PF00515 | 0.671 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3D3 | Leptomonas seymouri | 65% | 100% |
A0A0N0P3S4 | Leptomonas seymouri | 36% | 100% |
A0A0N1PA10 | Leptomonas seymouri | 30% | 100% |
A0A0N1PCQ2 | Leptomonas seymouri | 33% | 100% |
A0A0S4JQB3 | Bodo saltans | 30% | 100% |
A0A0S4KKL9 | Bodo saltans | 28% | 82% |
A0A1X0NSR3 | Trypanosomatidae | 29% | 97% |
A0A1X0NSS6 | Trypanosomatidae | 33% | 100% |
A0A1X0NT85 | Trypanosomatidae | 34% | 88% |
A0A3Q8IAY1 | Leishmania donovani | 37% | 100% |
A0A3R7KKJ0 | Trypanosoma rangeli | 33% | 100% |
A0A3S5IRR1 | Trypanosoma rangeli | 37% | 100% |
A0A3S7WUJ3 | Leishmania donovani | 30% | 100% |
A0A3S7WUK0 | Leishmania donovani | 93% | 100% |
A0A3S7X1K2 | Leishmania donovani | 31% | 100% |
A0A422NS41 | Trypanosoma rangeli | 30% | 100% |
A4H956 | Leishmania braziliensis | 33% | 100% |
A4H959 | Leishmania braziliensis | 77% | 100% |
A4H960 | Leishmania braziliensis | 35% | 100% |
A4HGL0 | Leishmania braziliensis | 31% | 100% |
A4HXH8 | Leishmania infantum | 31% | 100% |
A4HXI1 | Leishmania infantum | 92% | 100% |
A4HXI2 | Leishmania infantum | 37% | 100% |
A4I3N6 | Leishmania infantum | 32% | 100% |
C9ZP69 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
C9ZP70 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
E9AR73 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
E9AR76 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
E9AR77 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 37% | 100% |
E9AZX7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
Q4Q8A8 | Leishmania major | 32% | 97% |
Q4QE86 | Leishmania major | 38% | 100% |
Q54809 | Streptomyces peucetius | 26% | 100% |
Q55217 | Streptomyces sp. (strain C5) | 26% | 100% |
V5AZB9 | Trypanosoma cruzi | 30% | 100% |
V5BER0 | Trypanosoma cruzi | 33% | 100% |
V5BNU9 | Trypanosoma cruzi | 33% | 100% |