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:0031974 | membrane-enclosed lumen | 2 | 1 |
GO:0031981 | nuclear lumen | 5 | 1 |
GO:0032838 | plasma membrane bounded cell projection cytoplasm | 4 | 1 |
GO:0043233 | organelle lumen | 3 | 1 |
GO:0070013 | intracellular organelle lumen | 4 | 1 |
GO:0097014 | ciliary plasm | 5 | 1 |
GO:0099568 | cytoplasmic region | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9ASZ5
Term | Name | Level | Count |
---|---|---|---|
GO:0006470 | protein dephosphorylation | 5 | 7 |
GO:0006793 | phosphorus metabolic process | 3 | 7 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 7 |
GO:0006807 | nitrogen compound metabolic process | 2 | 7 |
GO:0008152 | metabolic process | 1 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0016311 | dephosphorylation | 5 | 7 |
GO:0019538 | protein metabolic process | 3 | 7 |
GO:0036211 | protein modification process | 4 | 7 |
GO:0043170 | macromolecule metabolic process | 3 | 7 |
GO:0043412 | macromolecule modification | 4 | 7 |
GO:0044237 | cellular metabolic process | 2 | 7 |
GO:0044238 | primary metabolic process | 2 | 7 |
GO:0071704 | organic substance metabolic process | 2 | 7 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 7 |
GO:0004721 | phosphoprotein phosphatase activity | 3 | 7 |
GO:0004725 | protein tyrosine phosphatase activity | 4 | 7 |
GO:0016787 | hydrolase activity | 2 | 7 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 7 |
GO:0016791 | phosphatase activity | 5 | 7 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 7 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 397 | 401 | PF00656 | 0.301 |
CLV_C14_Caspase3-7 | 406 | 410 | PF00656 | 0.237 |
CLV_C14_Caspase3-7 | 75 | 79 | PF00656 | 0.487 |
CLV_NRD_NRD_1 | 201 | 203 | PF00675 | 0.264 |
CLV_NRD_NRD_1 | 323 | 325 | PF00675 | 0.345 |
CLV_NRD_NRD_1 | 454 | 456 | PF00675 | 0.284 |
CLV_NRD_NRD_1 | 460 | 462 | PF00675 | 0.286 |
CLV_NRD_NRD_1 | 489 | 491 | PF00675 | 0.455 |
CLV_PCSK_KEX2_1 | 195 | 197 | PF00082 | 0.515 |
CLV_PCSK_KEX2_1 | 201 | 203 | PF00082 | 0.276 |
CLV_PCSK_KEX2_1 | 323 | 325 | PF00082 | 0.345 |
CLV_PCSK_KEX2_1 | 454 | 456 | PF00082 | 0.345 |
CLV_PCSK_KEX2_1 | 83 | 85 | PF00082 | 0.417 |
CLV_PCSK_PC1ET2_1 | 195 | 197 | PF00082 | 0.442 |
CLV_PCSK_PC1ET2_1 | 83 | 85 | PF00082 | 0.417 |
CLV_PCSK_SKI1_1 | 195 | 199 | PF00082 | 0.454 |
CLV_PCSK_SKI1_1 | 455 | 459 | PF00082 | 0.284 |
CLV_PCSK_SKI1_1 | 513 | 517 | PF00082 | 0.468 |
CLV_PCSK_SKI1_1 | 519 | 523 | PF00082 | 0.456 |
CLV_Separin_Metazoa | 320 | 324 | PF03568 | 0.345 |
DEG_SPOP_SBC_1 | 15 | 19 | PF00917 | 0.511 |
DOC_CKS1_1 | 375 | 380 | PF01111 | 0.181 |
DOC_CKS1_1 | 39 | 44 | PF01111 | 0.488 |
DOC_CYCLIN_RxL_1 | 192 | 200 | PF00134 | 0.434 |
DOC_CYCLIN_yCln2_LP_2 | 415 | 421 | PF00134 | 0.345 |
DOC_MAPK_MEF2A_6 | 414 | 421 | PF00069 | 0.284 |
DOC_MAPK_MEF2A_6 | 470 | 479 | PF00069 | 0.280 |
DOC_MAPK_RevD_3 | 475 | 491 | PF00069 | 0.393 |
DOC_PP1_RVXF_1 | 178 | 185 | PF00149 | 0.370 |
DOC_PP2B_LxvP_1 | 415 | 418 | PF13499 | 0.345 |
DOC_USP7_MATH_1 | 15 | 19 | PF00917 | 0.602 |
DOC_USP7_MATH_1 | 178 | 182 | PF00917 | 0.534 |
DOC_USP7_MATH_1 | 207 | 211 | PF00917 | 0.181 |
DOC_USP7_MATH_1 | 26 | 30 | PF00917 | 0.620 |
DOC_USP7_MATH_1 | 288 | 292 | PF00917 | 0.284 |
DOC_USP7_MATH_1 | 33 | 37 | PF00917 | 0.549 |
DOC_USP7_MATH_1 | 394 | 398 | PF00917 | 0.253 |
DOC_USP7_MATH_1 | 79 | 83 | PF00917 | 0.531 |
DOC_WW_Pin1_4 | 165 | 170 | PF00397 | 0.744 |
DOC_WW_Pin1_4 | 174 | 179 | PF00397 | 0.504 |
DOC_WW_Pin1_4 | 222 | 227 | PF00397 | 0.181 |
DOC_WW_Pin1_4 | 328 | 333 | PF00397 | 0.181 |
DOC_WW_Pin1_4 | 374 | 379 | PF00397 | 0.224 |
DOC_WW_Pin1_4 | 38 | 43 | PF00397 | 0.778 |
DOC_WW_Pin1_4 | 388 | 393 | PF00397 | 0.198 |
DOC_WW_Pin1_4 | 413 | 418 | PF00397 | 0.345 |
LIG_14-3-3_CanoR_1 | 150 | 155 | PF00244 | 0.550 |
LIG_14-3-3_CanoR_1 | 162 | 169 | PF00244 | 0.575 |
LIG_14-3-3_CanoR_1 | 20 | 25 | PF00244 | 0.622 |
LIG_14-3-3_CanoR_1 | 490 | 498 | PF00244 | 0.434 |
LIG_AP_GAE_1 | 105 | 111 | PF02883 | 0.434 |
LIG_APCC_ABBA_1 | 303 | 308 | PF00400 | 0.280 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.651 |
LIG_BRCT_BRCA1_1 | 180 | 184 | PF00533 | 0.365 |
LIG_eIF4E_1 | 229 | 235 | PF01652 | 0.181 |
LIG_FHA_1 | 216 | 222 | PF00498 | 0.471 |
LIG_FHA_1 | 265 | 271 | PF00498 | 0.345 |
LIG_FHA_1 | 316 | 322 | PF00498 | 0.290 |
LIG_FHA_1 | 414 | 420 | PF00498 | 0.383 |
LIG_FHA_1 | 428 | 434 | PF00498 | 0.252 |
LIG_FHA_1 | 68 | 74 | PF00498 | 0.588 |
LIG_FHA_2 | 235 | 241 | PF00498 | 0.312 |
LIG_FHA_2 | 271 | 277 | PF00498 | 0.298 |
LIG_FHA_2 | 404 | 410 | PF00498 | 0.290 |
LIG_LIR_Gen_1 | 255 | 262 | PF02991 | 0.345 |
LIG_LIR_Gen_1 | 358 | 368 | PF02991 | 0.280 |
LIG_LIR_Gen_1 | 472 | 482 | PF02991 | 0.321 |
LIG_LIR_Gen_1 | 98 | 109 | PF02991 | 0.363 |
LIG_LIR_Nem_3 | 105 | 111 | PF02991 | 0.306 |
LIG_LIR_Nem_3 | 255 | 260 | PF02991 | 0.458 |
LIG_LIR_Nem_3 | 358 | 364 | PF02991 | 0.280 |
LIG_LIR_Nem_3 | 387 | 393 | PF02991 | 0.191 |
LIG_LIR_Nem_3 | 472 | 477 | PF02991 | 0.321 |
LIG_LIR_Nem_3 | 89 | 93 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 98 | 104 | PF02991 | 0.328 |
LIG_MYND_1 | 11 | 15 | PF01753 | 0.508 |
LIG_NRP_CendR_1 | 522 | 523 | PF00754 | 0.535 |
LIG_PCNA_PIPBox_1 | 251 | 260 | PF02747 | 0.345 |
LIG_PTB_Apo_2 | 84 | 91 | PF02174 | 0.403 |
LIG_SH2_CRK | 344 | 348 | PF00017 | 0.345 |
LIG_SH2_CRK | 390 | 394 | PF00017 | 0.184 |
LIG_SH2_CRK | 437 | 441 | PF00017 | 0.280 |
LIG_SH2_CRK | 474 | 478 | PF00017 | 0.280 |
LIG_SH2_CRK | 93 | 97 | PF00017 | 0.420 |
LIG_SH2_GRB2like | 135 | 138 | PF00017 | 0.409 |
LIG_SH2_GRB2like | 229 | 232 | PF00017 | 0.280 |
LIG_SH2_NCK_1 | 390 | 394 | PF00017 | 0.184 |
LIG_SH2_PTP2 | 135 | 138 | PF00017 | 0.409 |
LIG_SH2_PTP2 | 327 | 330 | PF00017 | 0.345 |
LIG_SH2_SRC | 135 | 138 | PF00017 | 0.409 |
LIG_SH2_SRC | 229 | 232 | PF00017 | 0.345 |
LIG_SH2_SRC | 344 | 347 | PF00017 | 0.345 |
LIG_SH2_STAP1 | 262 | 266 | PF00017 | 0.345 |
LIG_SH2_STAP1 | 313 | 317 | PF00017 | 0.280 |
LIG_SH2_STAT5 | 135 | 138 | PF00017 | 0.409 |
LIG_SH2_STAT5 | 229 | 232 | PF00017 | 0.280 |
LIG_SH2_STAT5 | 313 | 316 | PF00017 | 0.280 |
LIG_SH2_STAT5 | 327 | 330 | PF00017 | 0.280 |
LIG_SH2_STAT5 | 346 | 349 | PF00017 | 0.168 |
LIG_SH2_STAT5 | 371 | 374 | PF00017 | 0.279 |
LIG_SH2_STAT5 | 437 | 440 | PF00017 | 0.280 |
LIG_SH2_STAT5 | 59 | 62 | PF00017 | 0.569 |
LIG_SH3_3 | 319 | 325 | PF00018 | 0.340 |
LIG_SH3_3 | 344 | 350 | PF00018 | 0.345 |
LIG_SH3_3 | 36 | 42 | PF00018 | 0.492 |
LIG_SH3_3 | 369 | 375 | PF00018 | 0.296 |
LIG_SH3_3 | 379 | 385 | PF00018 | 0.301 |
LIG_SH3_3 | 5 | 11 | PF00018 | 0.617 |
LIG_SUMO_SIM_anti_2 | 255 | 263 | PF11976 | 0.345 |
LIG_SUMO_SIM_anti_2 | 265 | 270 | PF11976 | 0.252 |
LIG_SUMO_SIM_par_1 | 267 | 274 | PF11976 | 0.284 |
LIG_TRAF2_1 | 140 | 143 | PF00917 | 0.363 |
LIG_TRAF2_1 | 249 | 252 | PF00917 | 0.345 |
LIG_TRAF2_1 | 360 | 363 | PF00917 | 0.280 |
LIG_TRAF2_1 | 96 | 99 | PF00917 | 0.544 |
LIG_TYR_ITIM | 342 | 347 | PF00017 | 0.345 |
LIG_WRC_WIRS_1 | 297 | 302 | PF05994 | 0.279 |
MOD_CDK_SPxK_1 | 174 | 180 | PF00069 | 0.546 |
MOD_CK1_1 | 161 | 167 | PF00069 | 0.619 |
MOD_CK1_1 | 168 | 174 | PF00069 | 0.573 |
MOD_CK1_1 | 18 | 24 | PF00069 | 0.632 |
MOD_CK1_1 | 29 | 35 | PF00069 | 0.532 |
MOD_CK1_1 | 299 | 305 | PF00069 | 0.301 |
MOD_CK1_1 | 331 | 337 | PF00069 | 0.345 |
MOD_CK1_1 | 357 | 363 | PF00069 | 0.280 |
MOD_CK1_1 | 6 | 12 | PF00069 | 0.590 |
MOD_CK1_1 | 69 | 75 | PF00069 | 0.624 |
MOD_CK2_1 | 18 | 24 | PF00069 | 0.633 |
MOD_CK2_1 | 234 | 240 | PF00069 | 0.301 |
MOD_CK2_1 | 270 | 276 | PF00069 | 0.280 |
MOD_CK2_1 | 357 | 363 | PF00069 | 0.280 |
MOD_CK2_1 | 79 | 85 | PF00069 | 0.488 |
MOD_Cter_Amidation | 193 | 196 | PF01082 | 0.371 |
MOD_GlcNHglycan | 165 | 168 | PF01048 | 0.588 |
MOD_GlcNHglycan | 173 | 176 | PF01048 | 0.528 |
MOD_GlcNHglycan | 289 | 293 | PF01048 | 0.293 |
MOD_GlcNHglycan | 31 | 34 | PF01048 | 0.629 |
MOD_GlcNHglycan | 35 | 38 | PF01048 | 0.596 |
MOD_GlcNHglycan | 386 | 389 | PF01048 | 0.311 |
MOD_GlcNHglycan | 396 | 399 | PF01048 | 0.224 |
MOD_GlcNHglycan | 423 | 426 | PF01048 | 0.262 |
MOD_GlcNHglycan | 48 | 51 | PF01048 | 0.544 |
MOD_GlcNHglycan | 492 | 495 | PF01048 | 0.443 |
MOD_GlcNHglycan | 55 | 58 | PF01048 | 0.565 |
MOD_GSK3_1 | 14 | 21 | PF00069 | 0.646 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.542 |
MOD_GSK3_1 | 154 | 161 | PF00069 | 0.599 |
MOD_GSK3_1 | 163 | 170 | PF00069 | 0.516 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.447 |
MOD_GSK3_1 | 215 | 222 | PF00069 | 0.240 |
MOD_GSK3_1 | 260 | 267 | PF00069 | 0.364 |
MOD_GSK3_1 | 29 | 36 | PF00069 | 0.490 |
MOD_GSK3_1 | 311 | 318 | PF00069 | 0.290 |
MOD_GSK3_1 | 37 | 44 | PF00069 | 0.669 |
MOD_GSK3_1 | 384 | 391 | PF00069 | 0.425 |
MOD_GSK3_1 | 399 | 406 | PF00069 | 0.217 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.536 |
MOD_GSK3_1 | 68 | 75 | PF00069 | 0.490 |
MOD_N-GLC_1 | 121 | 126 | PF02516 | 0.359 |
MOD_N-GLC_1 | 15 | 20 | PF02516 | 0.651 |
MOD_N-GLC_1 | 26 | 31 | PF02516 | 0.573 |
MOD_N-GLC_1 | 449 | 454 | PF02516 | 0.345 |
MOD_NEK2_1 | 123 | 128 | PF00069 | 0.394 |
MOD_NEK2_1 | 163 | 168 | PF00069 | 0.632 |
MOD_NEK2_1 | 197 | 202 | PF00069 | 0.283 |
MOD_NEK2_1 | 234 | 239 | PF00069 | 0.356 |
MOD_NEK2_1 | 243 | 248 | PF00069 | 0.276 |
MOD_NEK2_1 | 448 | 453 | PF00069 | 0.353 |
MOD_NEK2_1 | 66 | 71 | PF00069 | 0.592 |
MOD_PIKK_1 | 243 | 249 | PF00454 | 0.280 |
MOD_PIKK_1 | 331 | 337 | PF00454 | 0.301 |
MOD_PIKK_1 | 43 | 49 | PF00454 | 0.620 |
MOD_PK_1 | 150 | 156 | PF00069 | 0.463 |
MOD_PKA_1 | 490 | 496 | PF00069 | 0.448 |
MOD_PKA_2 | 161 | 167 | PF00069 | 0.582 |
MOD_PKA_2 | 19 | 25 | PF00069 | 0.539 |
MOD_PKA_2 | 207 | 213 | PF00069 | 0.195 |
MOD_PKA_2 | 6 | 12 | PF00069 | 0.612 |
MOD_Plk_1 | 111 | 117 | PF00069 | 0.402 |
MOD_Plk_1 | 141 | 147 | PF00069 | 0.391 |
MOD_Plk_1 | 235 | 241 | PF00069 | 0.345 |
MOD_Plk_1 | 26 | 32 | PF00069 | 0.590 |
MOD_Plk_1 | 264 | 270 | PF00069 | 0.459 |
MOD_Plk_1 | 3 | 9 | PF00069 | 0.653 |
MOD_Plk_1 | 449 | 455 | PF00069 | 0.352 |
MOD_Plk_2-3 | 311 | 317 | PF00069 | 0.254 |
MOD_Plk_4 | 141 | 147 | PF00069 | 0.358 |
MOD_Plk_4 | 26 | 32 | PF00069 | 0.505 |
MOD_Plk_4 | 264 | 270 | PF00069 | 0.344 |
MOD_Plk_4 | 429 | 435 | PF00069 | 0.280 |
MOD_Plk_4 | 72 | 78 | PF00069 | 0.469 |
MOD_ProDKin_1 | 165 | 171 | PF00069 | 0.742 |
MOD_ProDKin_1 | 174 | 180 | PF00069 | 0.499 |
MOD_ProDKin_1 | 222 | 228 | PF00069 | 0.181 |
MOD_ProDKin_1 | 328 | 334 | PF00069 | 0.181 |
MOD_ProDKin_1 | 374 | 380 | PF00069 | 0.224 |
MOD_ProDKin_1 | 38 | 44 | PF00069 | 0.778 |
MOD_ProDKin_1 | 388 | 394 | PF00069 | 0.198 |
MOD_ProDKin_1 | 413 | 419 | PF00069 | 0.345 |
TRG_DiLeu_BaEn_1 | 99 | 104 | PF01217 | 0.365 |
TRG_DiLeu_BaEn_2 | 275 | 281 | PF01217 | 0.345 |
TRG_DiLeu_BaEn_2 | 471 | 477 | PF01217 | 0.280 |
TRG_DiLeu_BaEn_3 | 362 | 368 | PF01217 | 0.280 |
TRG_DiLeu_BaLyEn_6 | 193 | 198 | PF01217 | 0.426 |
TRG_ENDOCYTIC_2 | 135 | 138 | PF00928 | 0.409 |
TRG_ENDOCYTIC_2 | 344 | 347 | PF00928 | 0.345 |
TRG_ENDOCYTIC_2 | 390 | 393 | PF00928 | 0.184 |
TRG_ENDOCYTIC_2 | 437 | 440 | PF00928 | 0.280 |
TRG_ENDOCYTIC_2 | 474 | 477 | PF00928 | 0.280 |
TRG_ENDOCYTIC_2 | 478 | 481 | PF00928 | 0.280 |
TRG_ER_diArg_1 | 322 | 324 | PF00400 | 0.345 |
TRG_ER_diArg_1 | 453 | 455 | PF00400 | 0.345 |
TRG_NES_CRM1_1 | 295 | 309 | PF08389 | 0.235 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1ILN6 | Leptomonas seymouri | 46% | 100% |
A0A3S7XAX7 | Leishmania donovani | 88% | 100% |
A4HP87 | Leishmania braziliensis | 76% | 100% |
A4IDJ2 | Leishmania infantum | 88% | 100% |
P34138 | Dictyostelium discoideum | 24% | 100% |
Q4Q1K3 | Leishmania major | 89% | 100% |