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: 7 |
NetGPI | no | yes: 0, no: 7 |
Related structures:
AlphaFold database: E9AZ21
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 8 |
GO:0004721 | phosphoprotein phosphatase activity | 3 | 8 |
GO:0004722 | protein serine/threonine phosphatase activity | 4 | 8 |
GO:0005488 | binding | 1 | 8 |
GO:0016787 | hydrolase activity | 2 | 8 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 8 |
GO:0016791 | phosphatase activity | 5 | 8 |
GO:0017018 | myosin phosphatase activity | 5 | 8 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 8 |
GO:0043167 | ion binding | 2 | 8 |
GO:0043169 | cation binding | 3 | 8 |
GO:0046872 | metal ion binding | 4 | 8 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 182 | 186 | PF00656 | 0.764 |
CLV_NRD_NRD_1 | 3 | 5 | PF00675 | 0.623 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.623 |
CLV_PCSK_SKI1_1 | 335 | 339 | PF00082 | 0.489 |
DEG_APCC_DBOX_1 | 334 | 342 | PF00400 | 0.592 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.688 |
DEG_SPOP_SBC_1 | 193 | 197 | PF00917 | 0.399 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 330 | 338 | PF00134 | 0.558 |
DOC_CYCLIN_yCln2_LP_2 | 246 | 252 | PF00134 | 0.533 |
DOC_MAPK_MEF2A_6 | 261 | 270 | PF00069 | 0.583 |
DOC_MAPK_MEF2A_6 | 384 | 392 | PF00069 | 0.481 |
DOC_PP2B_LxvP_1 | 266 | 269 | PF13499 | 0.564 |
DOC_PP4_FxxP_1 | 414 | 417 | PF00568 | 0.712 |
DOC_USP7_MATH_1 | 151 | 155 | PF00917 | 0.752 |
DOC_USP7_MATH_1 | 179 | 183 | PF00917 | 0.823 |
DOC_USP7_MATH_1 | 322 | 326 | PF00917 | 0.658 |
DOC_USP7_MATH_1 | 368 | 372 | PF00917 | 0.482 |
DOC_USP7_MATH_1 | 85 | 89 | PF00917 | 0.491 |
DOC_USP7_MATH_2 | 403 | 409 | PF00917 | 0.653 |
DOC_WW_Pin1_4 | 256 | 261 | PF00397 | 0.483 |
DOC_WW_Pin1_4 | 364 | 369 | PF00397 | 0.447 |
LIG_14-3-3_CanoR_1 | 205 | 215 | PF00244 | 0.534 |
LIG_14-3-3_CanoR_1 | 302 | 310 | PF00244 | 0.521 |
LIG_APCC_ABBA_1 | 296 | 301 | PF00400 | 0.550 |
LIG_Clathr_ClatBox_1 | 267 | 271 | PF01394 | 0.493 |
LIG_deltaCOP1_diTrp_1 | 294 | 304 | PF00928 | 0.476 |
LIG_EH1_1 | 289 | 297 | PF00400 | 0.429 |
LIG_eIF4E_1 | 75 | 81 | PF01652 | 0.518 |
LIG_FHA_1 | 107 | 113 | PF00498 | 0.454 |
LIG_FHA_1 | 138 | 144 | PF00498 | 0.508 |
LIG_FHA_1 | 161 | 167 | PF00498 | 0.704 |
LIG_FHA_1 | 194 | 200 | PF00498 | 0.563 |
LIG_FHA_1 | 224 | 230 | PF00498 | 0.390 |
LIG_FHA_1 | 278 | 284 | PF00498 | 0.529 |
LIG_FHA_1 | 387 | 393 | PF00498 | 0.466 |
LIG_FHA_2 | 112 | 118 | PF00498 | 0.483 |
LIG_FHA_2 | 176 | 182 | PF00498 | 0.646 |
LIG_FHA_2 | 189 | 195 | PF00498 | 0.589 |
LIG_FHA_2 | 257 | 263 | PF00498 | 0.514 |
LIG_FHA_2 | 334 | 340 | PF00498 | 0.580 |
LIG_Integrin_isoDGR_2 | 232 | 234 | PF01839 | 0.530 |
LIG_LIR_Apic_2 | 411 | 417 | PF02991 | 0.628 |
LIG_LIR_Gen_1 | 126 | 136 | PF02991 | 0.524 |
LIG_LIR_Gen_1 | 281 | 292 | PF02991 | 0.414 |
LIG_LIR_Gen_1 | 34 | 45 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 126 | 131 | PF02991 | 0.528 |
LIG_LIR_Nem_3 | 281 | 287 | PF02991 | 0.401 |
LIG_LIR_Nem_3 | 294 | 300 | PF02991 | 0.423 |
LIG_LIR_Nem_3 | 34 | 40 | PF02991 | 0.551 |
LIG_LIR_Nem_3 | 87 | 92 | PF02991 | 0.454 |
LIG_NRBOX | 333 | 339 | PF00104 | 0.541 |
LIG_PCNA_yPIPBox_3 | 330 | 338 | PF02747 | 0.558 |
LIG_REV1ctd_RIR_1 | 13 | 22 | PF16727 | 0.452 |
LIG_SH2_SRC | 73 | 76 | PF00017 | 0.467 |
LIG_SH2_STAP1 | 128 | 132 | PF00017 | 0.487 |
LIG_SH2_STAP1 | 64 | 68 | PF00017 | 0.420 |
LIG_SH2_STAT3 | 248 | 251 | PF00017 | 0.527 |
LIG_SH2_STAT5 | 215 | 218 | PF00017 | 0.490 |
LIG_SH2_STAT5 | 221 | 224 | PF00017 | 0.419 |
LIG_SH2_STAT5 | 237 | 240 | PF00017 | 0.571 |
LIG_SH2_STAT5 | 309 | 312 | PF00017 | 0.593 |
LIG_SH2_STAT5 | 75 | 78 | PF00017 | 0.504 |
LIG_SH3_3 | 133 | 139 | PF00018 | 0.664 |
LIG_SUMO_SIM_anti_2 | 129 | 134 | PF11976 | 0.497 |
LIG_SUMO_SIM_anti_2 | 274 | 281 | PF11976 | 0.403 |
LIG_SUMO_SIM_par_1 | 386 | 393 | PF11976 | 0.546 |
LIG_TRAF2_1 | 114 | 117 | PF00917 | 0.495 |
LIG_TRAF2_1 | 118 | 121 | PF00917 | 0.617 |
MOD_CDK_SPK_2 | 256 | 261 | PF00069 | 0.513 |
MOD_CK1_1 | 137 | 143 | PF00069 | 0.502 |
MOD_CK1_1 | 154 | 160 | PF00069 | 0.583 |
MOD_CK1_1 | 175 | 181 | PF00069 | 0.776 |
MOD_CK1_1 | 256 | 262 | PF00069 | 0.486 |
MOD_CK2_1 | 111 | 117 | PF00069 | 0.420 |
MOD_CK2_1 | 171 | 177 | PF00069 | 0.802 |
MOD_CK2_1 | 188 | 194 | PF00069 | 0.404 |
MOD_CK2_1 | 405 | 411 | PF00069 | 0.655 |
MOD_Cter_Amidation | 9 | 12 | PF01082 | 0.558 |
MOD_GlcNHglycan | 153 | 156 | PF01048 | 0.702 |
MOD_GlcNHglycan | 174 | 177 | PF01048 | 0.812 |
MOD_GlcNHglycan | 181 | 184 | PF01048 | 0.609 |
MOD_GlcNHglycan | 346 | 350 | PF01048 | 0.509 |
MOD_GlcNHglycan | 407 | 410 | PF01048 | 0.623 |
MOD_GlcNHglycan | 64 | 67 | PF01048 | 0.402 |
MOD_GSK3_1 | 137 | 144 | PF00069 | 0.549 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.753 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.721 |
MOD_GSK3_1 | 179 | 186 | PF00069 | 0.669 |
MOD_GSK3_1 | 188 | 195 | PF00069 | 0.492 |
MOD_GSK3_1 | 364 | 371 | PF00069 | 0.442 |
MOD_GSK3_1 | 386 | 393 | PF00069 | 0.465 |
MOD_GSK3_1 | 401 | 408 | PF00069 | 0.499 |
MOD_GSK3_1 | 95 | 102 | PF00069 | 0.576 |
MOD_N-GLC_1 | 256 | 261 | PF02516 | 0.526 |
MOD_NEK2_1 | 111 | 116 | PF00069 | 0.422 |
MOD_NEK2_1 | 150 | 155 | PF00069 | 0.786 |
MOD_NEK2_1 | 345 | 350 | PF00069 | 0.374 |
MOD_NEK2_1 | 38 | 43 | PF00069 | 0.487 |
MOD_NEK2_1 | 390 | 395 | PF00069 | 0.482 |
MOD_NEK2_2 | 85 | 90 | PF00069 | 0.497 |
MOD_NEK2_2 | 95 | 100 | PF00069 | 0.493 |
MOD_PIKK_1 | 302 | 308 | PF00454 | 0.389 |
MOD_PKA_1 | 11 | 17 | PF00069 | 0.441 |
MOD_Plk_1 | 169 | 175 | PF00069 | 0.794 |
MOD_Plk_1 | 223 | 229 | PF00069 | 0.389 |
MOD_Plk_1 | 386 | 392 | PF00069 | 0.419 |
MOD_Plk_2-3 | 181 | 187 | PF00069 | 0.733 |
MOD_Plk_4 | 223 | 229 | PF00069 | 0.442 |
MOD_Plk_4 | 386 | 392 | PF00069 | 0.419 |
MOD_Plk_4 | 48 | 54 | PF00069 | 0.468 |
MOD_ProDKin_1 | 256 | 262 | PF00069 | 0.486 |
MOD_ProDKin_1 | 364 | 370 | PF00069 | 0.442 |
TRG_DiLeu_BaLyEn_6 | 262 | 267 | PF01217 | 0.516 |
TRG_DiLeu_BaLyEn_6 | 87 | 92 | PF01217 | 0.481 |
TRG_ENDOCYTIC_2 | 128 | 131 | PF00928 | 0.503 |
TRG_ENDOCYTIC_2 | 73 | 76 | PF00928 | 0.409 |
TRG_ER_diArg_1 | 2 | 4 | PF00400 | 0.595 |
TRG_Pf-PMV_PEXEL_1 | 335 | 339 | PF00026 | 0.480 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PC93 | Leptomonas seymouri | 61% | 100% |
A0A0S4JF75 | Bodo saltans | 29% | 80% |
A0A3S7X0P0 | Leishmania donovani | 94% | 100% |
A4HFP3 | Leishmania braziliensis | 79% | 100% |
A4I2R9 | Leishmania infantum | 94% | 100% |
E9AD96 | Leishmania major | 92% | 100% |