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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9B448
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 7 |
GO:0016787 | hydrolase activity | 2 | 1 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 1 |
GO:0016791 | phosphatase activity | 5 | 1 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 192 | 196 | PF00656 | 0.714 |
CLV_C14_Caspase3-7 | 204 | 208 | PF00656 | 0.691 |
CLV_C14_Caspase3-7 | 446 | 450 | PF00656 | 0.733 |
CLV_C14_Caspase3-7 | 490 | 494 | PF00656 | 0.508 |
CLV_MEL_PAP_1 | 159 | 165 | PF00089 | 0.411 |
CLV_NRD_NRD_1 | 102 | 104 | PF00675 | 0.411 |
CLV_NRD_NRD_1 | 22 | 24 | PF00675 | 0.640 |
CLV_NRD_NRD_1 | 254 | 256 | PF00675 | 0.799 |
CLV_NRD_NRD_1 | 31 | 33 | PF00675 | 0.472 |
CLV_NRD_NRD_1 | 419 | 421 | PF00675 | 0.760 |
CLV_NRD_NRD_1 | 8 | 10 | PF00675 | 0.653 |
CLV_PCSK_FUR_1 | 417 | 421 | PF00082 | 0.589 |
CLV_PCSK_KEX2_1 | 102 | 104 | PF00082 | 0.411 |
CLV_PCSK_KEX2_1 | 22 | 24 | PF00082 | 0.622 |
CLV_PCSK_KEX2_1 | 254 | 256 | PF00082 | 0.751 |
CLV_PCSK_KEX2_1 | 31 | 33 | PF00082 | 0.472 |
CLV_PCSK_KEX2_1 | 419 | 421 | PF00082 | 0.596 |
CLV_PCSK_KEX2_1 | 427 | 429 | PF00082 | 0.599 |
CLV_PCSK_KEX2_1 | 7 | 9 | PF00082 | 0.655 |
CLV_PCSK_KEX2_1 | 73 | 75 | PF00082 | 0.411 |
CLV_PCSK_PC1ET2_1 | 427 | 429 | PF00082 | 0.565 |
CLV_PCSK_PC1ET2_1 | 73 | 75 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 140 | 144 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 22 | 26 | PF00082 | 0.502 |
CLV_PCSK_SKI1_1 | 277 | 281 | PF00082 | 0.707 |
CLV_PCSK_SKI1_1 | 31 | 35 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 349 | 353 | PF00082 | 0.473 |
DEG_APCC_DBOX_1 | 94 | 102 | PF00400 | 0.383 |
DEG_MDM2_SWIB_1 | 307 | 314 | PF02201 | 0.411 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.761 |
DEG_SPOP_SBC_1 | 246 | 250 | PF00917 | 0.807 |
DEG_SPOP_SBC_1 | 421 | 425 | PF00917 | 0.657 |
DOC_CYCLIN_RxL_1 | 346 | 355 | PF00134 | 0.508 |
DOC_MAPK_gen_1 | 310 | 318 | PF00069 | 0.411 |
DOC_MAPK_gen_1 | 93 | 101 | PF00069 | 0.222 |
DOC_MAPK_MEF2A_6 | 172 | 179 | PF00069 | 0.530 |
DOC_MAPK_NFAT4_5 | 172 | 180 | PF00069 | 0.535 |
DOC_PP2B_LxvP_1 | 177 | 180 | PF13499 | 0.632 |
DOC_PP4_FxxP_1 | 312 | 315 | PF00568 | 0.411 |
DOC_USP7_MATH_1 | 246 | 250 | PF00917 | 0.702 |
DOC_USP7_MATH_1 | 404 | 408 | PF00917 | 0.730 |
DOC_USP7_MATH_1 | 421 | 425 | PF00917 | 0.571 |
DOC_USP7_MATH_1 | 426 | 430 | PF00917 | 0.769 |
DOC_USP7_MATH_1 | 431 | 435 | PF00917 | 0.681 |
DOC_USP7_MATH_1 | 448 | 452 | PF00917 | 0.535 |
DOC_WW_Pin1_4 | 209 | 214 | PF00397 | 0.559 |
DOC_WW_Pin1_4 | 216 | 221 | PF00397 | 0.523 |
DOC_WW_Pin1_4 | 237 | 242 | PF00397 | 0.817 |
DOC_WW_Pin1_4 | 427 | 432 | PF00397 | 0.830 |
DOC_WW_Pin1_4 | 476 | 481 | PF00397 | 0.763 |
DOC_WW_Pin1_4 | 50 | 55 | PF00397 | 0.360 |
DOC_WW_Pin1_4 | 86 | 91 | PF00397 | 0.411 |
LIG_14-3-3_CanoR_1 | 102 | 106 | PF00244 | 0.411 |
LIG_14-3-3_CanoR_1 | 23 | 29 | PF00244 | 0.563 |
LIG_14-3-3_CanoR_1 | 258 | 262 | PF00244 | 0.648 |
LIG_14-3-3_CanoR_1 | 341 | 351 | PF00244 | 0.497 |
LIG_14-3-3_CanoR_1 | 93 | 99 | PF00244 | 0.411 |
LIG_Actin_RPEL_3 | 16 | 35 | PF02755 | 0.401 |
LIG_Actin_WH2_2 | 156 | 174 | PF00022 | 0.513 |
LIG_BRCT_BRCA1_1 | 163 | 167 | PF00533 | 0.411 |
LIG_deltaCOP1_diTrp_1 | 134 | 143 | PF00928 | 0.389 |
LIG_deltaCOP1_diTrp_1 | 367 | 376 | PF00928 | 0.570 |
LIG_FHA_2 | 202 | 208 | PF00498 | 0.704 |
LIG_FHA_2 | 95 | 101 | PF00498 | 0.411 |
LIG_GBD_Chelix_1 | 298 | 306 | PF00786 | 0.411 |
LIG_LIR_Apic_2 | 53 | 59 | PF02991 | 0.411 |
LIG_LIR_Gen_1 | 164 | 175 | PF02991 | 0.411 |
LIG_LIR_Gen_1 | 317 | 326 | PF02991 | 0.411 |
LIG_LIR_Gen_1 | 483 | 492 | PF02991 | 0.645 |
LIG_LIR_Nem_3 | 164 | 170 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 374 | 379 | PF02991 | 0.700 |
LIG_LIR_Nem_3 | 483 | 487 | PF02991 | 0.684 |
LIG_LIR_Nem_3 | 82 | 88 | PF02991 | 0.411 |
LIG_MLH1_MIPbox_1 | 163 | 167 | PF16413 | 0.411 |
LIG_Pex14_2 | 307 | 311 | PF04695 | 0.411 |
LIG_SH2_CRK | 127 | 131 | PF00017 | 0.513 |
LIG_SH2_CRK | 148 | 152 | PF00017 | 0.411 |
LIG_SH2_GRB2like | 50 | 53 | PF00017 | 0.513 |
LIG_SH2_STAT5 | 11 | 14 | PF00017 | 0.461 |
LIG_SH2_STAT5 | 85 | 88 | PF00017 | 0.411 |
LIG_SH3_2 | 412 | 417 | PF14604 | 0.812 |
LIG_SH3_3 | 207 | 213 | PF00018 | 0.511 |
LIG_SH3_3 | 222 | 228 | PF00018 | 0.494 |
LIG_SH3_3 | 259 | 265 | PF00018 | 0.638 |
LIG_SH3_3 | 406 | 412 | PF00018 | 0.647 |
LIG_SH3_3 | 466 | 472 | PF00018 | 0.600 |
LIG_SH3_5 | 480 | 484 | PF00018 | 0.707 |
LIG_SH3_CIN85_PxpxPR_1 | 412 | 417 | PF14604 | 0.812 |
LIG_SUMO_SIM_par_1 | 329 | 334 | PF11976 | 0.411 |
LIG_TRAF2_1 | 220 | 223 | PF00917 | 0.525 |
LIG_TRAF2_1 | 385 | 388 | PF00917 | 0.765 |
LIG_TRAF2_2 | 129 | 134 | PF00917 | 0.436 |
LIG_WW_3 | 414 | 418 | PF00397 | 0.823 |
MOD_CDK_SPxK_1 | 476 | 482 | PF00069 | 0.708 |
MOD_CDK_SPxxK_3 | 50 | 57 | PF00069 | 0.411 |
MOD_CDK_SPxxK_3 | 86 | 93 | PF00069 | 0.411 |
MOD_CK1_1 | 422 | 428 | PF00069 | 0.809 |
MOD_CK1_1 | 429 | 435 | PF00069 | 0.853 |
MOD_CK1_1 | 438 | 444 | PF00069 | 0.593 |
MOD_CK1_1 | 451 | 457 | PF00069 | 0.608 |
MOD_CK2_1 | 101 | 107 | PF00069 | 0.411 |
MOD_CK2_1 | 285 | 291 | PF00069 | 0.389 |
MOD_CK2_1 | 440 | 446 | PF00069 | 0.837 |
MOD_CK2_1 | 94 | 100 | PF00069 | 0.411 |
MOD_Cter_Amidation | 71 | 74 | PF01082 | 0.411 |
MOD_GlcNHglycan | 154 | 157 | PF01048 | 0.355 |
MOD_GlcNHglycan | 163 | 166 | PF01048 | 0.357 |
MOD_GlcNHglycan | 233 | 236 | PF01048 | 0.816 |
MOD_GlcNHglycan | 249 | 252 | PF01048 | 0.559 |
MOD_GlcNHglycan | 406 | 409 | PF01048 | 0.627 |
MOD_GlcNHglycan | 433 | 436 | PF01048 | 0.739 |
MOD_GlcNHglycan | 439 | 443 | PF01048 | 0.741 |
MOD_GlcNHglycan | 446 | 449 | PF01048 | 0.788 |
MOD_GlcNHglycan | 450 | 453 | PF01048 | 0.539 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.390 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.616 |
MOD_GSK3_1 | 201 | 208 | PF00069 | 0.613 |
MOD_GSK3_1 | 214 | 221 | PF00069 | 0.674 |
MOD_GSK3_1 | 227 | 234 | PF00069 | 0.800 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.829 |
MOD_GSK3_1 | 253 | 260 | PF00069 | 0.545 |
MOD_GSK3_1 | 422 | 429 | PF00069 | 0.761 |
MOD_GSK3_1 | 431 | 438 | PF00069 | 0.761 |
MOD_GSK3_1 | 440 | 447 | PF00069 | 0.509 |
MOD_N-GLC_2 | 183 | 185 | PF02516 | 0.736 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.719 |
MOD_NEK2_1 | 105 | 110 | PF00069 | 0.381 |
MOD_NEK2_1 | 152 | 157 | PF00069 | 0.411 |
MOD_NEK2_1 | 166 | 171 | PF00069 | 0.411 |
MOD_NEK2_1 | 253 | 258 | PF00069 | 0.696 |
MOD_PIKK_1 | 105 | 111 | PF00454 | 0.411 |
MOD_PIKK_1 | 218 | 224 | PF00454 | 0.822 |
MOD_PKA_1 | 419 | 425 | PF00069 | 0.854 |
MOD_PKA_2 | 101 | 107 | PF00069 | 0.411 |
MOD_PKA_2 | 161 | 167 | PF00069 | 0.411 |
MOD_PKA_2 | 171 | 177 | PF00069 | 0.411 |
MOD_PKA_2 | 253 | 259 | PF00069 | 0.695 |
MOD_PKA_2 | 419 | 425 | PF00069 | 0.562 |
MOD_PKA_2 | 94 | 100 | PF00069 | 0.411 |
MOD_PKB_1 | 417 | 425 | PF00069 | 0.851 |
MOD_Plk_1 | 105 | 111 | PF00069 | 0.411 |
MOD_Plk_1 | 133 | 139 | PF00069 | 0.411 |
MOD_Plk_1 | 366 | 372 | PF00069 | 0.563 |
MOD_Plk_4 | 166 | 172 | PF00069 | 0.429 |
MOD_Plk_4 | 24 | 30 | PF00069 | 0.613 |
MOD_Plk_4 | 94 | 100 | PF00069 | 0.222 |
MOD_ProDKin_1 | 209 | 215 | PF00069 | 0.562 |
MOD_ProDKin_1 | 216 | 222 | PF00069 | 0.524 |
MOD_ProDKin_1 | 237 | 243 | PF00069 | 0.815 |
MOD_ProDKin_1 | 427 | 433 | PF00069 | 0.830 |
MOD_ProDKin_1 | 476 | 482 | PF00069 | 0.762 |
MOD_ProDKin_1 | 50 | 56 | PF00069 | 0.360 |
MOD_ProDKin_1 | 86 | 92 | PF00069 | 0.411 |
MOD_SUMO_rev_2 | 51 | 59 | PF00179 | 0.411 |
TRG_DiLeu_BaEn_1 | 292 | 297 | PF01217 | 0.319 |
TRG_DiLeu_BaLyEn_6 | 29 | 34 | PF01217 | 0.469 |
TRG_DiLeu_BaLyEn_6 | 353 | 358 | PF01217 | 0.524 |
TRG_ENDOCYTIC_2 | 127 | 130 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 147 | 150 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 484 | 487 | PF00928 | 0.725 |
TRG_ER_diArg_1 | 101 | 103 | PF00400 | 0.411 |
TRG_ER_diArg_1 | 22 | 24 | PF00400 | 0.622 |
TRG_ER_diArg_1 | 253 | 255 | PF00400 | 0.798 |
TRG_ER_diArg_1 | 30 | 32 | PF00400 | 0.479 |
TRG_ER_diArg_1 | 416 | 419 | PF00400 | 0.752 |
TRG_ER_diArg_1 | 7 | 9 | PF00400 | 0.655 |
TRG_Pf-PMV_PEXEL_1 | 76 | 80 | PF00026 | 0.411 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IHK5 | Leptomonas seymouri | 66% | 100% |
A0A3Q8IU44 | Leishmania donovani | 90% | 100% |
A4HLS2 | Leishmania braziliensis | 79% | 100% |
A4I981 | Leishmania infantum | 90% | 100% |
Q4Q3X7 | Leishmania major | 90% | 100% |