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: 5 |
NetGPI | no | yes: 0, no: 5 |
Related structures:
AlphaFold database: E9B6N1
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 1 |
GO:0004721 | phosphoprotein phosphatase activity | 3 | 1 |
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 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 123 | 125 | PF00675 | 0.756 |
CLV_NRD_NRD_1 | 424 | 426 | PF00675 | 0.433 |
CLV_NRD_NRD_1 | 451 | 453 | PF00675 | 0.573 |
CLV_NRD_NRD_1 | 471 | 473 | PF00675 | 0.481 |
CLV_NRD_NRD_1 | 69 | 71 | PF00675 | 0.666 |
CLV_PCSK_FUR_1 | 67 | 71 | PF00082 | 0.539 |
CLV_PCSK_KEX2_1 | 110 | 112 | PF00082 | 0.817 |
CLV_PCSK_KEX2_1 | 123 | 125 | PF00082 | 0.580 |
CLV_PCSK_KEX2_1 | 424 | 426 | PF00082 | 0.433 |
CLV_PCSK_KEX2_1 | 451 | 453 | PF00082 | 0.680 |
CLV_PCSK_KEX2_1 | 69 | 71 | PF00082 | 0.571 |
CLV_PCSK_PC1ET2_1 | 110 | 112 | PF00082 | 0.817 |
CLV_PCSK_SKI1_1 | 316 | 320 | PF00082 | 0.252 |
CLV_PCSK_SKI1_1 | 425 | 429 | PF00082 | 0.433 |
DOC_MAPK_gen_1 | 123 | 130 | PF00069 | 0.599 |
DOC_MAPK_gen_1 | 32 | 40 | PF00069 | 0.520 |
DOC_MAPK_gen_1 | 421 | 429 | PF00069 | 0.530 |
DOC_MAPK_MEF2A_6 | 276 | 283 | PF00069 | 0.512 |
DOC_MAPK_MEF2A_6 | 32 | 40 | PF00069 | 0.520 |
DOC_MAPK_MEF2A_6 | 366 | 375 | PF00069 | 0.522 |
DOC_MAPK_MEF2A_6 | 508 | 516 | PF00069 | 0.608 |
DOC_PP1_RVXF_1 | 536 | 543 | PF00149 | 0.650 |
DOC_PP2B_PxIxI_1 | 368 | 374 | PF00149 | 0.620 |
DOC_USP7_MATH_1 | 115 | 119 | PF00917 | 0.714 |
DOC_USP7_MATH_1 | 122 | 126 | PF00917 | 0.723 |
DOC_USP7_MATH_1 | 42 | 46 | PF00917 | 0.510 |
DOC_USP7_MATH_1 | 440 | 444 | PF00917 | 0.433 |
DOC_USP7_MATH_1 | 487 | 491 | PF00917 | 0.692 |
DOC_USP7_UBL2_3 | 324 | 328 | PF12436 | 0.530 |
DOC_WW_Pin1_4 | 161 | 166 | PF00397 | 0.630 |
DOC_WW_Pin1_4 | 175 | 180 | PF00397 | 0.642 |
DOC_WW_Pin1_4 | 183 | 188 | PF00397 | 0.640 |
DOC_WW_Pin1_4 | 208 | 213 | PF00397 | 0.704 |
DOC_WW_Pin1_4 | 253 | 258 | PF00397 | 0.481 |
DOC_WW_Pin1_4 | 265 | 270 | PF00397 | 0.406 |
DOC_WW_Pin1_4 | 403 | 408 | PF00397 | 0.437 |
DOC_WW_Pin1_4 | 473 | 478 | PF00397 | 0.517 |
DOC_WW_Pin1_4 | 53 | 58 | PF00397 | 0.624 |
LIG_14-3-3_CanoR_1 | 116 | 121 | PF00244 | 0.755 |
LIG_14-3-3_CanoR_1 | 123 | 129 | PF00244 | 0.682 |
LIG_14-3-3_CanoR_1 | 13 | 22 | PF00244 | 0.621 |
LIG_14-3-3_CanoR_1 | 188 | 195 | PF00244 | 0.684 |
LIG_14-3-3_CanoR_1 | 213 | 218 | PF00244 | 0.627 |
LIG_14-3-3_CanoR_1 | 276 | 280 | PF00244 | 0.478 |
LIG_14-3-3_CanoR_1 | 525 | 533 | PF00244 | 0.582 |
LIG_BIR_III_2 | 192 | 196 | PF00653 | 0.629 |
LIG_BIR_III_4 | 310 | 314 | PF00653 | 0.238 |
LIG_DLG_GKlike_1 | 124 | 131 | PF00625 | 0.732 |
LIG_FHA_1 | 21 | 27 | PF00498 | 0.730 |
LIG_FHA_1 | 276 | 282 | PF00498 | 0.501 |
LIG_FHA_1 | 288 | 294 | PF00498 | 0.430 |
LIG_FHA_1 | 424 | 430 | PF00498 | 0.467 |
LIG_FHA_1 | 487 | 493 | PF00498 | 0.786 |
LIG_FHA_1 | 509 | 515 | PF00498 | 0.601 |
LIG_FHA_1 | 54 | 60 | PF00498 | 0.733 |
LIG_FHA_1 | 86 | 92 | PF00498 | 0.674 |
LIG_FHA_2 | 100 | 106 | PF00498 | 0.530 |
LIG_FHA_2 | 218 | 224 | PF00498 | 0.775 |
LIG_FHA_2 | 480 | 486 | PF00498 | 0.733 |
LIG_LIR_Gen_1 | 334 | 344 | PF02991 | 0.530 |
LIG_LIR_Gen_1 | 500 | 510 | PF02991 | 0.567 |
LIG_LIR_Nem_3 | 101 | 107 | PF02991 | 0.659 |
LIG_LIR_Nem_3 | 203 | 209 | PF02991 | 0.541 |
LIG_LIR_Nem_3 | 320 | 326 | PF02991 | 0.462 |
LIG_LIR_Nem_3 | 334 | 339 | PF02991 | 0.366 |
LIG_LIR_Nem_3 | 367 | 371 | PF02991 | 0.368 |
LIG_LIR_Nem_3 | 500 | 506 | PF02991 | 0.580 |
LIG_MYND_1 | 265 | 269 | PF01753 | 0.526 |
LIG_PCNA_TLS_4 | 330 | 337 | PF02747 | 0.530 |
LIG_PCNA_yPIPBox_3 | 424 | 438 | PF02747 | 0.530 |
LIG_PTB_Apo_2 | 257 | 264 | PF02174 | 0.644 |
LIG_RPA_C_Fungi | 119 | 131 | PF08784 | 0.605 |
LIG_RPA_C_Fungi | 58 | 70 | PF08784 | 0.539 |
LIG_SH2_CRK | 22 | 26 | PF00017 | 0.521 |
LIG_SH2_CRK | 441 | 445 | PF00017 | 0.530 |
LIG_SH2_STAP1 | 356 | 360 | PF00017 | 0.530 |
LIG_SH2_STAP1 | 412 | 416 | PF00017 | 0.433 |
LIG_SH2_STAP1 | 501 | 505 | PF00017 | 0.378 |
LIG_SH2_STAT5 | 22 | 25 | PF00017 | 0.522 |
LIG_SH2_STAT5 | 266 | 269 | PF00017 | 0.482 |
LIG_SH2_STAT5 | 335 | 338 | PF00017 | 0.275 |
LIG_SH2_STAT5 | 43 | 46 | PF00017 | 0.611 |
LIG_SH2_STAT5 | 501 | 504 | PF00017 | 0.395 |
LIG_SH3_1 | 22 | 28 | PF00018 | 0.519 |
LIG_SH3_3 | 204 | 210 | PF00018 | 0.609 |
LIG_SH3_3 | 22 | 28 | PF00018 | 0.796 |
LIG_SH3_3 | 290 | 296 | PF00018 | 0.396 |
LIG_SH3_3 | 434 | 440 | PF00018 | 0.530 |
LIG_SUMO_SIM_anti_2 | 125 | 133 | PF11976 | 0.694 |
LIG_SUMO_SIM_par_1 | 277 | 282 | PF11976 | 0.530 |
LIG_SUMO_SIM_par_1 | 425 | 430 | PF11976 | 0.530 |
LIG_TRAF2_1 | 219 | 222 | PF00917 | 0.677 |
LIG_WRC_WIRS_1 | 532 | 537 | PF05994 | 0.718 |
MOD_CDC14_SPxK_1 | 164 | 167 | PF00782 | 0.721 |
MOD_CDK_SPK_2 | 183 | 188 | PF00069 | 0.595 |
MOD_CDK_SPK_2 | 208 | 213 | PF00069 | 0.611 |
MOD_CDK_SPxK_1 | 161 | 167 | PF00069 | 0.629 |
MOD_CDK_SPxxK_3 | 175 | 182 | PF00069 | 0.544 |
MOD_CDK_SPxxK_3 | 265 | 272 | PF00069 | 0.442 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.761 |
MOD_CK1_1 | 201 | 207 | PF00069 | 0.717 |
MOD_CK1_1 | 317 | 323 | PF00069 | 0.433 |
MOD_CK1_1 | 378 | 384 | PF00069 | 0.788 |
MOD_CK1_1 | 479 | 485 | PF00069 | 0.748 |
MOD_CK1_1 | 98 | 104 | PF00069 | 0.702 |
MOD_CK2_1 | 217 | 223 | PF00069 | 0.780 |
MOD_CK2_1 | 238 | 244 | PF00069 | 0.424 |
MOD_CK2_1 | 479 | 485 | PF00069 | 0.816 |
MOD_CK2_1 | 524 | 530 | PF00069 | 0.665 |
MOD_CK2_1 | 99 | 105 | PF00069 | 0.530 |
MOD_Cter_Amidation | 108 | 111 | PF01082 | 0.819 |
MOD_GlcNHglycan | 107 | 110 | PF01048 | 0.737 |
MOD_GlcNHglycan | 17 | 20 | PF01048 | 0.714 |
MOD_GlcNHglycan | 319 | 322 | PF01048 | 0.504 |
MOD_GlcNHglycan | 380 | 383 | PF01048 | 0.786 |
MOD_GlcNHglycan | 44 | 47 | PF01048 | 0.609 |
MOD_GlcNHglycan | 478 | 481 | PF01048 | 0.832 |
MOD_GlcNHglycan | 517 | 520 | PF01048 | 0.360 |
MOD_GSK3_1 | 156 | 163 | PF00069 | 0.692 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.523 |
MOD_GSK3_1 | 201 | 208 | PF00069 | 0.616 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.673 |
MOD_GSK3_1 | 283 | 290 | PF00069 | 0.407 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.812 |
MOD_GSK3_1 | 376 | 383 | PF00069 | 0.582 |
MOD_GSK3_1 | 472 | 479 | PF00069 | 0.713 |
MOD_GSK3_1 | 85 | 92 | PF00069 | 0.571 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.708 |
MOD_N-GLC_1 | 253 | 258 | PF02516 | 0.604 |
MOD_N-GLC_1 | 430 | 435 | PF02516 | 0.238 |
MOD_N-GLC_1 | 94 | 99 | PF02516 | 0.783 |
MOD_NEK2_1 | 238 | 243 | PF00069 | 0.513 |
MOD_NEK2_1 | 283 | 288 | PF00069 | 0.530 |
MOD_NEK2_1 | 30 | 35 | PF00069 | 0.714 |
MOD_NEK2_1 | 349 | 354 | PF00069 | 0.530 |
MOD_NEK2_1 | 36 | 41 | PF00069 | 0.643 |
MOD_NEK2_1 | 375 | 380 | PF00069 | 0.642 |
MOD_NEK2_1 | 423 | 428 | PF00069 | 0.530 |
MOD_NEK2_1 | 536 | 541 | PF00069 | 0.742 |
MOD_NEK2_1 | 99 | 104 | PF00069 | 0.704 |
MOD_NEK2_2 | 440 | 445 | PF00069 | 0.433 |
MOD_PIKK_1 | 384 | 390 | PF00454 | 0.702 |
MOD_PIKK_1 | 524 | 530 | PF00454 | 0.568 |
MOD_PKA_1 | 123 | 129 | PF00069 | 0.661 |
MOD_PKA_1 | 472 | 478 | PF00069 | 0.516 |
MOD_PKA_1 | 69 | 75 | PF00069 | 0.536 |
MOD_PKA_2 | 115 | 121 | PF00069 | 0.685 |
MOD_PKA_2 | 12 | 18 | PF00069 | 0.618 |
MOD_PKA_2 | 122 | 128 | PF00069 | 0.722 |
MOD_PKA_2 | 275 | 281 | PF00069 | 0.413 |
MOD_PKA_2 | 423 | 429 | PF00069 | 0.530 |
MOD_PKA_2 | 524 | 530 | PF00069 | 0.568 |
MOD_PKA_2 | 62 | 68 | PF00069 | 0.537 |
MOD_PKA_2 | 69 | 75 | PF00069 | 0.522 |
MOD_PKB_1 | 114 | 122 | PF00069 | 0.715 |
MOD_PKB_1 | 67 | 75 | PF00069 | 0.536 |
MOD_Plk_1 | 283 | 289 | PF00069 | 0.407 |
MOD_Plk_1 | 430 | 436 | PF00069 | 0.238 |
MOD_Plk_1 | 487 | 493 | PF00069 | 0.714 |
MOD_Plk_1 | 508 | 514 | PF00069 | 0.611 |
MOD_Plk_1 | 74 | 80 | PF00069 | 0.821 |
MOD_Plk_1 | 94 | 100 | PF00069 | 0.686 |
MOD_Plk_4 | 213 | 219 | PF00069 | 0.752 |
MOD_Plk_4 | 275 | 281 | PF00069 | 0.501 |
MOD_Plk_4 | 283 | 289 | PF00069 | 0.362 |
MOD_Plk_4 | 508 | 514 | PF00069 | 0.611 |
MOD_Plk_4 | 531 | 537 | PF00069 | 0.720 |
MOD_Plk_4 | 74 | 80 | PF00069 | 0.530 |
MOD_ProDKin_1 | 161 | 167 | PF00069 | 0.629 |
MOD_ProDKin_1 | 175 | 181 | PF00069 | 0.644 |
MOD_ProDKin_1 | 183 | 189 | PF00069 | 0.639 |
MOD_ProDKin_1 | 208 | 214 | PF00069 | 0.703 |
MOD_ProDKin_1 | 253 | 259 | PF00069 | 0.485 |
MOD_ProDKin_1 | 265 | 271 | PF00069 | 0.411 |
MOD_ProDKin_1 | 403 | 409 | PF00069 | 0.437 |
MOD_ProDKin_1 | 473 | 479 | PF00069 | 0.520 |
MOD_ProDKin_1 | 53 | 59 | PF00069 | 0.625 |
MOD_SUMO_for_1 | 166 | 169 | PF00179 | 0.632 |
TRG_DiLeu_BaEn_1 | 509 | 514 | PF01217 | 0.598 |
TRG_DiLeu_BaLyEn_6 | 234 | 239 | PF01217 | 0.658 |
TRG_DiLeu_BaLyEn_6 | 54 | 59 | PF01217 | 0.636 |
TRG_ENDOCYTIC_2 | 104 | 107 | PF00928 | 0.636 |
TRG_ENDOCYTIC_2 | 323 | 326 | PF00928 | 0.530 |
TRG_ENDOCYTIC_2 | 441 | 444 | PF00928 | 0.530 |
TRG_ENDOCYTIC_2 | 503 | 506 | PF00928 | 0.548 |
TRG_ER_diArg_1 | 423 | 425 | PF00400 | 0.433 |
TRG_ER_diArg_1 | 67 | 70 | PF00400 | 0.575 |
TRG_Pf-PMV_PEXEL_1 | 188 | 192 | PF00026 | 0.736 |
TRG_Pf-PMV_PEXEL_1 | 362 | 367 | PF00026 | 0.530 |
TRG_Pf-PMV_PEXEL_1 | 49 | 53 | PF00026 | 0.723 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IIK2 | Leishmania donovani | 79% | 98% |
A4HN21 | Leishmania braziliensis | 62% | 93% |
A4IBP7 | Leishmania infantum | 80% | 98% |
E9AFH6 | Leishmania major | 80% | 100% |