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: 25 |
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: 8 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 33 |
NetGPI | no | yes: 0, no: 33 |
Related structures:
AlphaFold database: E9AZV7
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 30 |
GO:0016787 | hydrolase activity | 2 | 30 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 2 | 6 | PF00656 | 0.470 |
CLV_NRD_NRD_1 | 15 | 17 | PF00675 | 0.633 |
CLV_NRD_NRD_1 | 377 | 379 | PF00675 | 0.303 |
CLV_NRD_NRD_1 | 81 | 83 | PF00675 | 0.275 |
CLV_PCSK_FUR_1 | 78 | 82 | PF00082 | 0.346 |
CLV_PCSK_KEX2_1 | 15 | 17 | PF00082 | 0.465 |
CLV_PCSK_KEX2_1 | 277 | 279 | PF00082 | 0.259 |
CLV_PCSK_KEX2_1 | 80 | 82 | PF00082 | 0.263 |
CLV_PCSK_PC1ET2_1 | 277 | 279 | PF00082 | 0.303 |
CLV_PCSK_PC1ET2_1 | 80 | 82 | PF00082 | 0.284 |
CLV_PCSK_SKI1_1 | 267 | 271 | PF00082 | 0.271 |
CLV_PCSK_SKI1_1 | 277 | 281 | PF00082 | 0.290 |
CLV_PCSK_SKI1_1 | 359 | 363 | PF00082 | 0.209 |
CLV_PCSK_SKI1_1 | 52 | 56 | PF00082 | 0.320 |
CLV_PCSK_SKI1_1 | 71 | 75 | PF00082 | 0.194 |
DEG_APCC_DBOX_1 | 51 | 59 | PF00400 | 0.525 |
DEG_SCF_FBW7_1 | 123 | 130 | PF00400 | 0.509 |
DEG_SCF_FBW7_1 | 99 | 105 | PF00400 | 0.410 |
DOC_CKS1_1 | 124 | 129 | PF01111 | 0.506 |
DOC_CKS1_1 | 92 | 97 | PF01111 | 0.651 |
DOC_CKS1_1 | 99 | 104 | PF01111 | 0.653 |
DOC_CYCLIN_RxL_1 | 356 | 366 | PF00134 | 0.400 |
DOC_MAPK_DCC_7 | 357 | 367 | PF00069 | 0.422 |
DOC_MAPK_gen_1 | 15 | 22 | PF00069 | 0.631 |
DOC_MAPK_gen_1 | 357 | 367 | PF00069 | 0.485 |
DOC_MAPK_gen_1 | 78 | 85 | PF00069 | 0.539 |
DOC_MAPK_MEF2A_6 | 359 | 367 | PF00069 | 0.448 |
DOC_MAPK_MEF2A_6 | 90 | 99 | PF00069 | 0.640 |
DOC_USP7_MATH_1 | 102 | 106 | PF00917 | 0.768 |
DOC_USP7_MATH_1 | 116 | 120 | PF00917 | 0.722 |
DOC_USP7_MATH_1 | 125 | 129 | PF00917 | 0.681 |
DOC_USP7_MATH_1 | 148 | 152 | PF00917 | 0.539 |
DOC_USP7_MATH_1 | 265 | 269 | PF00917 | 0.565 |
DOC_USP7_MATH_1 | 396 | 400 | PF00917 | 0.718 |
DOC_WW_Pin1_4 | 112 | 117 | PF00397 | 0.737 |
DOC_WW_Pin1_4 | 123 | 128 | PF00397 | 0.645 |
DOC_WW_Pin1_4 | 91 | 96 | PF00397 | 0.619 |
DOC_WW_Pin1_4 | 98 | 103 | PF00397 | 0.624 |
LIG_14-3-3_CanoR_1 | 237 | 241 | PF00244 | 0.484 |
LIG_14-3-3_CanoR_1 | 254 | 261 | PF00244 | 0.564 |
LIG_14-3-3_CanoR_1 | 378 | 386 | PF00244 | 0.596 |
LIG_14-3-3_CanoR_1 | 71 | 79 | PF00244 | 0.499 |
LIG_14-3-3_CterR_2 | 398 | 401 | PF00244 | 0.438 |
LIG_Actin_WH2_2 | 383 | 400 | PF00022 | 0.344 |
LIG_APCC_ABBA_1 | 361 | 366 | PF00400 | 0.387 |
LIG_BRCT_BRCA1_1 | 255 | 259 | PF00533 | 0.546 |
LIG_BRCT_BRCA1_1 | 380 | 384 | PF00533 | 0.300 |
LIG_EVH1_1 | 123 | 127 | PF00568 | 0.503 |
LIG_FHA_1 | 137 | 143 | PF00498 | 0.678 |
LIG_FHA_1 | 237 | 243 | PF00498 | 0.545 |
LIG_FHA_1 | 247 | 253 | PF00498 | 0.443 |
LIG_FHA_1 | 297 | 303 | PF00498 | 0.522 |
LIG_FHA_1 | 49 | 55 | PF00498 | 0.479 |
LIG_FHA_1 | 87 | 93 | PF00498 | 0.585 |
LIG_FHA_2 | 323 | 329 | PF00498 | 0.482 |
LIG_FHA_2 | 99 | 105 | PF00498 | 0.653 |
LIG_IBAR_NPY_1 | 27 | 29 | PF08397 | 0.342 |
LIG_LIR_Gen_1 | 176 | 185 | PF02991 | 0.498 |
LIG_LIR_Nem_3 | 176 | 181 | PF02991 | 0.498 |
LIG_LIR_Nem_3 | 239 | 243 | PF02991 | 0.518 |
LIG_LIR_Nem_3 | 257 | 263 | PF02991 | 0.485 |
LIG_MYND_3 | 362 | 366 | PF01753 | 0.437 |
LIG_NRBOX | 54 | 60 | PF00104 | 0.541 |
LIG_Pex14_1 | 220 | 224 | PF04695 | 0.503 |
LIG_SH2_CRK | 205 | 209 | PF00017 | 0.537 |
LIG_SH2_CRK | 29 | 33 | PF00017 | 0.342 |
LIG_SH2_GRB2like | 205 | 208 | PF00017 | 0.559 |
LIG_SH2_NCK_1 | 157 | 161 | PF00017 | 0.541 |
LIG_SH2_NCK_1 | 205 | 209 | PF00017 | 0.587 |
LIG_SH2_STAP1 | 165 | 169 | PF00017 | 0.526 |
LIG_SH2_STAP1 | 178 | 182 | PF00017 | 0.463 |
LIG_SH2_STAP1 | 50 | 54 | PF00017 | 0.548 |
LIG_SH2_STAT5 | 205 | 208 | PF00017 | 0.504 |
LIG_SH2_STAT5 | 300 | 303 | PF00017 | 0.580 |
LIG_SH2_STAT5 | 50 | 53 | PF00017 | 0.476 |
LIG_SH3_3 | 119 | 125 | PF00018 | 0.507 |
LIG_SH3_3 | 17 | 23 | PF00018 | 0.651 |
LIG_SH3_3 | 96 | 102 | PF00018 | 0.628 |
LIG_SUMO_SIM_anti_2 | 338 | 344 | PF11976 | 0.509 |
LIG_TRAF2_1 | 216 | 219 | PF00917 | 0.491 |
MOD_CDK_SPxxK_3 | 103 | 110 | PF00069 | 0.519 |
MOD_CK1_1 | 105 | 111 | PF00069 | 0.738 |
MOD_CK1_1 | 115 | 121 | PF00069 | 0.720 |
MOD_CK1_1 | 129 | 135 | PF00069 | 0.580 |
MOD_CK1_1 | 236 | 242 | PF00069 | 0.535 |
MOD_CK1_1 | 307 | 313 | PF00069 | 0.479 |
MOD_CK1_1 | 43 | 49 | PF00069 | 0.479 |
MOD_CK2_1 | 191 | 197 | PF00069 | 0.585 |
MOD_CK2_1 | 241 | 247 | PF00069 | 0.458 |
MOD_CK2_1 | 98 | 104 | PF00069 | 0.650 |
MOD_GlcNHglycan | 112 | 115 | PF01048 | 0.739 |
MOD_GlcNHglycan | 131 | 134 | PF01048 | 0.613 |
MOD_GlcNHglycan | 266 | 270 | PF01048 | 0.186 |
MOD_GlcNHglycan | 296 | 299 | PF01048 | 0.304 |
MOD_GlcNHglycan | 312 | 315 | PF01048 | 0.240 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.741 |
MOD_GSK3_1 | 123 | 130 | PF00069 | 0.655 |
MOD_GSK3_1 | 36 | 43 | PF00069 | 0.502 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.641 |
MOD_N-GLC_1 | 116 | 121 | PF02516 | 0.530 |
MOD_N-GLC_1 | 136 | 141 | PF02516 | 0.487 |
MOD_N-GLC_1 | 43 | 48 | PF02516 | 0.310 |
MOD_NEK2_1 | 147 | 152 | PF00069 | 0.501 |
MOD_NEK2_1 | 246 | 251 | PF00069 | 0.555 |
MOD_NEK2_1 | 288 | 293 | PF00069 | 0.531 |
MOD_NEK2_1 | 322 | 327 | PF00069 | 0.489 |
MOD_NEK2_1 | 341 | 346 | PF00069 | 0.538 |
MOD_NEK2_1 | 36 | 41 | PF00069 | 0.473 |
MOD_NEK2_1 | 86 | 91 | PF00069 | 0.410 |
MOD_PKA_1 | 378 | 384 | PF00069 | 0.456 |
MOD_PKA_2 | 236 | 242 | PF00069 | 0.500 |
MOD_PKA_2 | 253 | 259 | PF00069 | 0.543 |
MOD_Plk_1 | 165 | 171 | PF00069 | 0.552 |
MOD_Plk_1 | 246 | 252 | PF00069 | 0.386 |
MOD_Plk_1 | 265 | 271 | PF00069 | 0.421 |
MOD_Plk_1 | 288 | 294 | PF00069 | 0.531 |
MOD_Plk_1 | 322 | 328 | PF00069 | 0.491 |
MOD_Plk_1 | 43 | 49 | PF00069 | 0.451 |
MOD_Plk_2-3 | 214 | 220 | PF00069 | 0.541 |
MOD_Plk_4 | 118 | 124 | PF00069 | 0.529 |
MOD_Plk_4 | 176 | 182 | PF00069 | 0.484 |
MOD_Plk_4 | 36 | 42 | PF00069 | 0.479 |
MOD_Plk_4 | 8 | 14 | PF00069 | 0.586 |
MOD_ProDKin_1 | 112 | 118 | PF00069 | 0.738 |
MOD_ProDKin_1 | 123 | 129 | PF00069 | 0.646 |
MOD_ProDKin_1 | 91 | 97 | PF00069 | 0.624 |
MOD_ProDKin_1 | 98 | 104 | PF00069 | 0.634 |
MOD_SUMO_for_1 | 286 | 289 | PF00179 | 0.382 |
MOD_SUMO_rev_2 | 209 | 217 | PF00179 | 0.556 |
MOD_SUMO_rev_2 | 281 | 288 | PF00179 | 0.559 |
TRG_DiLeu_BaEn_1 | 266 | 271 | PF01217 | 0.389 |
TRG_ENDOCYTIC_2 | 178 | 181 | PF00928 | 0.451 |
TRG_ENDOCYTIC_2 | 29 | 32 | PF00928 | 0.344 |
TRG_ER_diArg_1 | 15 | 17 | PF00400 | 0.468 |
TRG_ER_diArg_1 | 81 | 83 | PF00400 | 0.420 |
TRG_NLS_MonoExtN_4 | 78 | 84 | PF00514 | 0.546 |
TRG_Pf-PMV_PEXEL_1 | 378 | 382 | PF00026 | 0.277 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7I9 | Leptomonas seymouri | 30% | 100% |
A0A0N0P7W9 | Leptomonas seymouri | 25% | 100% |
A0A0N1I1D8 | Leptomonas seymouri | 31% | 100% |
A0A0N1ILU0 | Leptomonas seymouri | 28% | 100% |
A0A0N1PEM6 | Leptomonas seymouri | 65% | 100% |
A0A1X0NRL0 | Trypanosomatidae | 26% | 100% |
A0A1X0NYN3 | Trypanosomatidae | 30% | 100% |
A0A1X0NYY3 | Trypanosomatidae | 30% | 100% |
A0A1X0P2Q4 | Trypanosomatidae | 39% | 100% |
A0A3Q8IDX0 | Leishmania donovani | 28% | 100% |
A0A3Q8IEU6 | Leishmania donovani | 93% | 100% |
A0A3Q8IGR3 | Leishmania donovani | 29% | 100% |
A0A3R7M7Z1 | Trypanosoma rangeli | 27% | 100% |
A0A3S7X1G8 | Leishmania donovani | 29% | 100% |
A0A422MX56 | Trypanosoma rangeli | 28% | 100% |
A0A422N4F0 | Trypanosoma rangeli | 30% | 100% |
A4HGI1 | Leishmania braziliensis | 27% | 90% |
A4HGI6 | Leishmania braziliensis | 29% | 83% |
A4HGI9 | Leishmania braziliensis | 28% | 100% |
A4HGJ0 | Leishmania braziliensis | 31% | 93% |
A4I3L4 | Leishmania infantum | 28% | 100% |
A4I3L6 | Leishmania infantum | 32% | 100% |
A4I3L7 | Leishmania infantum | 93% | 100% |
D0A7S2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
D0A841 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
E9AZV4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 86% |
E9AZV6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
Q4Q8C8 | Leishmania major | 93% | 100% |
Q4Q8C9 | Leishmania major | 29% | 100% |
Q4Q8D0 | Leishmania major | 24% | 79% |
Q4Q8D1 | Leishmania major | 30% | 86% |
V5BGL5 | Trypanosoma cruzi | 32% | 100% |