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 |
Related structures:
AlphaFold database: A0A3S7WX61
Term | Name | Level | Count |
---|---|---|---|
GO:0006473 | protein acetylation | 6 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0036211 | protein modification process | 4 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0043543 | protein acylation | 5 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 7 |
GO:0008080 | N-acetyltransferase activity | 6 | 7 |
GO:0016407 | acetyltransferase activity | 5 | 7 |
GO:0016410 | N-acyltransferase activity | 5 | 7 |
GO:0016740 | transferase activity | 2 | 7 |
GO:0016746 | acyltransferase activity | 3 | 7 |
GO:0016747 | acyltransferase activity, transferring groups other than amino-acyl groups | 4 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 275 | 279 | PF00656 | 0.529 |
CLV_NRD_NRD_1 | 131 | 133 | PF00675 | 0.648 |
CLV_NRD_NRD_1 | 248 | 250 | PF00675 | 0.639 |
CLV_NRD_NRD_1 | 295 | 297 | PF00675 | 0.287 |
CLV_NRD_NRD_1 | 336 | 338 | PF00675 | 0.346 |
CLV_NRD_NRD_1 | 405 | 407 | PF00675 | 0.626 |
CLV_NRD_NRD_1 | 413 | 415 | PF00675 | 0.554 |
CLV_PCSK_FUR_1 | 129 | 133 | PF00082 | 0.622 |
CLV_PCSK_KEX2_1 | 131 | 133 | PF00082 | 0.648 |
CLV_PCSK_KEX2_1 | 214 | 216 | PF00082 | 0.627 |
CLV_PCSK_KEX2_1 | 248 | 250 | PF00082 | 0.639 |
CLV_PCSK_KEX2_1 | 295 | 297 | PF00082 | 0.287 |
CLV_PCSK_KEX2_1 | 335 | 337 | PF00082 | 0.346 |
CLV_PCSK_KEX2_1 | 405 | 407 | PF00082 | 0.626 |
CLV_PCSK_KEX2_1 | 413 | 415 | PF00082 | 0.554 |
CLV_PCSK_PC1ET2_1 | 214 | 216 | PF00082 | 0.630 |
CLV_PCSK_SKI1_1 | 222 | 226 | PF00082 | 0.599 |
CLV_PCSK_SKI1_1 | 248 | 252 | PF00082 | 0.643 |
CLV_PCSK_SKI1_1 | 25 | 29 | PF00082 | 0.500 |
CLV_PCSK_SKI1_1 | 385 | 389 | PF00082 | 0.523 |
CLV_PCSK_SKI1_1 | 487 | 491 | PF00082 | 0.701 |
DEG_APCC_DBOX_1 | 31 | 39 | PF00400 | 0.434 |
DEG_APCC_DBOX_1 | 5 | 13 | PF00400 | 0.604 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.596 |
DEG_ODPH_VHL_1 | 317 | 329 | PF01847 | 0.567 |
DOC_CDC14_PxL_1 | 49 | 57 | PF14671 | 0.472 |
DOC_CKS1_1 | 310 | 315 | PF01111 | 0.620 |
DOC_CYCLIN_RxL_1 | 219 | 228 | PF00134 | 0.626 |
DOC_CYCLIN_RxL_1 | 22 | 30 | PF00134 | 0.492 |
DOC_CYCLIN_yCln2_LP_2 | 103 | 109 | PF00134 | 0.506 |
DOC_CYCLIN_yCln2_LP_2 | 251 | 257 | PF00134 | 0.470 |
DOC_MAPK_gen_1 | 385 | 395 | PF00069 | 0.581 |
DOC_MAPK_HePTP_8 | 246 | 258 | PF00069 | 0.410 |
DOC_MAPK_MEF2A_6 | 249 | 258 | PF00069 | 0.472 |
DOC_MAPK_MEF2A_6 | 321 | 329 | PF00069 | 0.620 |
DOC_PP1_RVXF_1 | 376 | 382 | PF00149 | 0.490 |
DOC_PP2B_LxvP_1 | 103 | 106 | PF13499 | 0.476 |
DOC_PP2B_LxvP_1 | 172 | 175 | PF13499 | 0.549 |
DOC_PP4_FxxP_1 | 170 | 173 | PF00568 | 0.707 |
DOC_PP4_FxxP_1 | 283 | 286 | PF00568 | 0.462 |
DOC_PP4_MxPP_1 | 148 | 151 | PF00568 | 0.563 |
DOC_USP7_MATH_1 | 157 | 161 | PF00917 | 0.756 |
DOC_USP7_MATH_1 | 163 | 167 | PF00917 | 0.670 |
DOC_USP7_MATH_1 | 175 | 179 | PF00917 | 0.611 |
DOC_USP7_MATH_1 | 302 | 306 | PF00917 | 0.604 |
DOC_USP7_MATH_1 | 420 | 424 | PF00917 | 0.649 |
DOC_USP7_MATH_1 | 74 | 78 | PF00917 | 0.563 |
DOC_USP7_MATH_2 | 199 | 205 | PF00917 | 0.577 |
DOC_WW_Pin1_4 | 159 | 164 | PF00397 | 0.721 |
DOC_WW_Pin1_4 | 195 | 200 | PF00397 | 0.705 |
DOC_WW_Pin1_4 | 294 | 299 | PF00397 | 0.593 |
DOC_WW_Pin1_4 | 305 | 310 | PF00397 | 0.489 |
DOC_WW_Pin1_4 | 4 | 9 | PF00397 | 0.610 |
DOC_WW_Pin1_4 | 455 | 460 | PF00397 | 0.749 |
LIG_14-3-3_CanoR_1 | 11 | 17 | PF00244 | 0.585 |
LIG_14-3-3_CanoR_1 | 191 | 199 | PF00244 | 0.665 |
LIG_14-3-3_CanoR_1 | 202 | 207 | PF00244 | 0.784 |
LIG_14-3-3_CanoR_1 | 296 | 304 | PF00244 | 0.593 |
LIG_14-3-3_CanoR_1 | 32 | 36 | PF00244 | 0.461 |
LIG_APCC_ABBA_1 | 372 | 377 | PF00400 | 0.537 |
LIG_APCC_ABBA_1 | 381 | 386 | PF00400 | 0.519 |
LIG_APCC_ABBA_1 | 387 | 392 | PF00400 | 0.553 |
LIG_BRCT_BRCA1_1 | 319 | 323 | PF00533 | 0.546 |
LIG_Clathr_ClatBox_1 | 263 | 267 | PF01394 | 0.567 |
LIG_EH1_1 | 322 | 330 | PF00400 | 0.546 |
LIG_FHA_1 | 188 | 194 | PF00498 | 0.754 |
LIG_FHA_1 | 320 | 326 | PF00498 | 0.546 |
LIG_FHA_1 | 356 | 362 | PF00498 | 0.546 |
LIG_FHA_1 | 367 | 373 | PF00498 | 0.546 |
LIG_FHA_1 | 374 | 380 | PF00498 | 0.601 |
LIG_FHA_1 | 98 | 104 | PF00498 | 0.475 |
LIG_FHA_2 | 183 | 189 | PF00498 | 0.639 |
LIG_FHA_2 | 190 | 196 | PF00498 | 0.723 |
LIG_FHA_2 | 399 | 405 | PF00498 | 0.526 |
LIG_FHA_2 | 73 | 79 | PF00498 | 0.564 |
LIG_HCF-1_HBM_1 | 40 | 43 | PF13415 | 0.437 |
LIG_LIR_Apic_2 | 169 | 173 | PF02991 | 0.681 |
LIG_LIR_Apic_2 | 472 | 477 | PF02991 | 0.787 |
LIG_LIR_Gen_1 | 100 | 109 | PF02991 | 0.490 |
LIG_LIR_Nem_3 | 100 | 104 | PF02991 | 0.458 |
LIG_MYND_1 | 309 | 313 | PF01753 | 0.541 |
LIG_MYND_1 | 53 | 57 | PF01753 | 0.558 |
LIG_MYND_3 | 149 | 153 | PF01753 | 0.710 |
LIG_Pex14_2 | 206 | 210 | PF04695 | 0.567 |
LIG_RPA_C_Fungi | 332 | 344 | PF08784 | 0.404 |
LIG_SH2_PTP2 | 255 | 258 | PF00017 | 0.452 |
LIG_SH2_SRC | 216 | 219 | PF00017 | 0.731 |
LIG_SH2_SRC | 43 | 46 | PF00017 | 0.395 |
LIG_SH2_STAP1 | 350 | 354 | PF00017 | 0.412 |
LIG_SH2_STAT5 | 255 | 258 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 43 | 46 | PF00017 | 0.469 |
LIG_SH2_STAT5 | 54 | 57 | PF00017 | 0.485 |
LIG_SH3_1 | 54 | 60 | PF00018 | 0.558 |
LIG_SH3_3 | 174 | 180 | PF00018 | 0.776 |
LIG_SH3_3 | 230 | 236 | PF00018 | 0.599 |
LIG_SH3_3 | 30 | 36 | PF00018 | 0.546 |
LIG_SH3_3 | 307 | 313 | PF00018 | 0.514 |
LIG_SH3_3 | 448 | 454 | PF00018 | 0.830 |
LIG_SH3_3 | 47 | 53 | PF00018 | 0.416 |
LIG_SH3_3 | 54 | 60 | PF00018 | 0.475 |
LIG_SUMO_SIM_anti_2 | 324 | 329 | PF11976 | 0.412 |
LIG_SUMO_SIM_anti_2 | 46 | 53 | PF11976 | 0.538 |
LIG_SUMO_SIM_par_1 | 75 | 85 | PF11976 | 0.530 |
LIG_TRAF2_1 | 151 | 154 | PF00917 | 0.716 |
LIG_TRAF2_1 | 81 | 84 | PF00917 | 0.528 |
LIG_WRC_WIRS_1 | 167 | 172 | PF05994 | 0.708 |
MOD_CDK_SPK_2 | 195 | 200 | PF00069 | 0.601 |
MOD_CDK_SPxxK_3 | 195 | 202 | PF00069 | 0.699 |
MOD_CDK_SPxxK_3 | 4 | 11 | PF00069 | 0.608 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.510 |
MOD_CK1_1 | 166 | 172 | PF00069 | 0.686 |
MOD_CK1_1 | 182 | 188 | PF00069 | 0.711 |
MOD_CK1_1 | 227 | 233 | PF00069 | 0.671 |
MOD_CK1_1 | 297 | 303 | PF00069 | 0.482 |
MOD_CK1_1 | 305 | 311 | PF00069 | 0.401 |
MOD_CK1_1 | 398 | 404 | PF00069 | 0.629 |
MOD_CK1_1 | 423 | 429 | PF00069 | 0.698 |
MOD_CK1_1 | 467 | 473 | PF00069 | 0.683 |
MOD_CK2_1 | 189 | 195 | PF00069 | 0.705 |
MOD_CK2_1 | 284 | 290 | PF00069 | 0.413 |
MOD_CK2_1 | 398 | 404 | PF00069 | 0.525 |
MOD_CK2_1 | 72 | 78 | PF00069 | 0.551 |
MOD_GlcNHglycan | 114 | 117 | PF01048 | 0.660 |
MOD_GlcNHglycan | 12 | 15 | PF01048 | 0.585 |
MOD_GlcNHglycan | 17 | 20 | PF01048 | 0.520 |
MOD_GlcNHglycan | 230 | 233 | PF01048 | 0.710 |
MOD_GlcNHglycan | 299 | 302 | PF01048 | 0.440 |
MOD_GlcNHglycan | 314 | 317 | PF01048 | 0.247 |
MOD_GlcNHglycan | 455 | 458 | PF01048 | 0.785 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.472 |
MOD_GSK3_1 | 155 | 162 | PF00069 | 0.690 |
MOD_GSK3_1 | 175 | 182 | PF00069 | 0.723 |
MOD_GSK3_1 | 183 | 190 | PF00069 | 0.641 |
MOD_GSK3_1 | 191 | 198 | PF00069 | 0.529 |
MOD_GSK3_1 | 223 | 230 | PF00069 | 0.630 |
MOD_GSK3_1 | 305 | 312 | PF00069 | 0.380 |
MOD_GSK3_1 | 364 | 371 | PF00069 | 0.391 |
MOD_GSK3_1 | 455 | 462 | PF00069 | 0.852 |
MOD_GSK3_1 | 74 | 81 | PF00069 | 0.560 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.520 |
MOD_LATS_1 | 189 | 195 | PF00433 | 0.569 |
MOD_LATS_1 | 294 | 300 | PF00433 | 0.404 |
MOD_NEK2_1 | 10 | 15 | PF00069 | 0.591 |
MOD_NEK2_1 | 21 | 26 | PF00069 | 0.479 |
MOD_NEK2_1 | 469 | 474 | PF00069 | 0.725 |
MOD_PIKK_1 | 216 | 222 | PF00454 | 0.730 |
MOD_PIKK_1 | 231 | 237 | PF00454 | 0.535 |
MOD_PIKK_1 | 459 | 465 | PF00454 | 0.767 |
MOD_PIKK_1 | 487 | 493 | PF00454 | 0.727 |
MOD_PKA_2 | 10 | 16 | PF00069 | 0.590 |
MOD_PKA_2 | 120 | 126 | PF00069 | 0.719 |
MOD_PKA_2 | 201 | 207 | PF00069 | 0.777 |
MOD_PKA_2 | 31 | 37 | PF00069 | 0.452 |
MOD_PKA_2 | 412 | 418 | PF00069 | 0.581 |
MOD_PKA_2 | 445 | 451 | PF00069 | 0.730 |
MOD_PKB_1 | 200 | 208 | PF00069 | 0.721 |
MOD_Plk_2-3 | 78 | 84 | PF00069 | 0.559 |
MOD_Plk_4 | 12 | 18 | PF00069 | 0.579 |
MOD_Plk_4 | 179 | 185 | PF00069 | 0.582 |
MOD_Plk_4 | 469 | 475 | PF00069 | 0.691 |
MOD_Plk_4 | 88 | 94 | PF00069 | 0.511 |
MOD_Plk_4 | 97 | 103 | PF00069 | 0.482 |
MOD_ProDKin_1 | 159 | 165 | PF00069 | 0.721 |
MOD_ProDKin_1 | 195 | 201 | PF00069 | 0.702 |
MOD_ProDKin_1 | 294 | 300 | PF00069 | 0.478 |
MOD_ProDKin_1 | 305 | 311 | PF00069 | 0.332 |
MOD_ProDKin_1 | 4 | 10 | PF00069 | 0.610 |
MOD_ProDKin_1 | 455 | 461 | PF00069 | 0.750 |
TRG_DiLeu_BaEn_1 | 40 | 45 | PF01217 | 0.585 |
TRG_DiLeu_BaEn_1 | 47 | 52 | PF01217 | 0.446 |
TRG_DiLeu_BaLyEn_6 | 208 | 213 | PF01217 | 0.630 |
TRG_DiLeu_LyEn_5 | 5 | 10 | PF01217 | 0.609 |
TRG_ENDOCYTIC_2 | 255 | 258 | PF00928 | 0.452 |
TRG_ER_diArg_1 | 129 | 132 | PF00400 | 0.685 |
TRG_ER_diArg_1 | 334 | 337 | PF00400 | 0.412 |
TRG_ER_diArg_1 | 413 | 416 | PF00400 | 0.558 |
TRG_Pf-PMV_PEXEL_1 | 249 | 253 | PF00026 | 0.594 |
TRG_Pf-PMV_PEXEL_1 | 25 | 29 | PF00026 | 0.556 |
TRG_Pf-PMV_PEXEL_1 | 337 | 341 | PF00026 | 0.412 |
TRG_Pf-PMV_PEXEL_1 | 345 | 349 | PF00026 | 0.412 |
TRG_Pf-PMV_PEXEL_1 | 397 | 402 | PF00026 | 0.614 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4Y0 | Leptomonas seymouri | 42% | 100% |
A4HCA5 | Leishmania braziliensis | 68% | 100% |
A4HZT7 | Leishmania infantum | 100% | 100% |
E9AVP2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
Q4QBT7 | Leishmania major | 89% | 100% |