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: A4HCA5
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 | 266 | 270 | PF00656 | 0.541 |
CLV_NRD_NRD_1 | 210 | 212 | PF00675 | 0.521 |
CLV_NRD_NRD_1 | 298 | 300 | PF00675 | 0.276 |
CLV_NRD_NRD_1 | 367 | 369 | PF00675 | 0.577 |
CLV_NRD_NRD_1 | 375 | 377 | PF00675 | 0.519 |
CLV_NRD_NRD_1 | 84 | 86 | PF00675 | 0.652 |
CLV_PCSK_KEX2_1 | 176 | 178 | PF00082 | 0.508 |
CLV_PCSK_KEX2_1 | 210 | 212 | PF00082 | 0.521 |
CLV_PCSK_KEX2_1 | 297 | 299 | PF00082 | 0.276 |
CLV_PCSK_KEX2_1 | 339 | 341 | PF00082 | 0.308 |
CLV_PCSK_KEX2_1 | 367 | 369 | PF00082 | 0.558 |
CLV_PCSK_KEX2_1 | 375 | 377 | PF00082 | 0.465 |
CLV_PCSK_KEX2_1 | 84 | 86 | PF00082 | 0.614 |
CLV_PCSK_PC1ET2_1 | 176 | 178 | PF00082 | 0.511 |
CLV_PCSK_PC1ET2_1 | 339 | 341 | PF00082 | 0.308 |
CLV_PCSK_SKI1_1 | 184 | 188 | PF00082 | 0.496 |
CLV_PCSK_SKI1_1 | 210 | 214 | PF00082 | 0.522 |
CLV_PCSK_SKI1_1 | 347 | 351 | PF00082 | 0.409 |
CLV_PCSK_SKI1_1 | 450 | 454 | PF00082 | 0.641 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.367 |
DEG_SCF_FBW7_1 | 272 | 278 | PF00400 | 0.524 |
DEG_SPOP_SBC_1 | 264 | 268 | PF00917 | 0.542 |
DOC_CKS1_1 | 272 | 277 | PF01111 | 0.689 |
DOC_CYCLIN_RxL_1 | 181 | 190 | PF00134 | 0.520 |
DOC_CYCLIN_yCln2_LP_2 | 14 | 20 | PF00134 | 0.266 |
DOC_CYCLIN_yCln2_LP_2 | 213 | 219 | PF00134 | 0.398 |
DOC_CYCLIN_yCln2_LP_2 | 67 | 73 | PF00134 | 0.409 |
DOC_MAPK_gen_1 | 339 | 346 | PF00069 | 0.405 |
DOC_MAPK_gen_1 | 347 | 357 | PF00069 | 0.453 |
DOC_MAPK_MEF2A_6 | 211 | 220 | PF00069 | 0.397 |
DOC_MAPK_MEF2A_6 | 283 | 291 | PF00069 | 0.533 |
DOC_PP1_RVXF_1 | 337 | 344 | PF00149 | 0.525 |
DOC_PP2B_LxvP_1 | 14 | 17 | PF13499 | 0.255 |
DOC_PP2B_LxvP_1 | 67 | 70 | PF13499 | 0.407 |
DOC_USP7_MATH_1 | 165 | 169 | PF00917 | 0.517 |
DOC_USP7_MATH_1 | 191 | 195 | PF00917 | 0.479 |
DOC_USP7_MATH_1 | 264 | 268 | PF00917 | 0.742 |
DOC_USP7_MATH_1 | 275 | 279 | PF00917 | 0.271 |
DOC_USP7_MATH_1 | 38 | 42 | PF00917 | 0.448 |
DOC_USP7_MATH_1 | 404 | 408 | PF00917 | 0.623 |
DOC_USP7_MATH_1 | 444 | 448 | PF00917 | 0.490 |
DOC_USP7_UBL2_3 | 325 | 329 | PF12436 | 0.416 |
DOC_WW_Pin1_4 | 246 | 251 | PF00397 | 0.592 |
DOC_WW_Pin1_4 | 256 | 261 | PF00397 | 0.673 |
DOC_WW_Pin1_4 | 268 | 273 | PF00397 | 0.574 |
DOC_WW_Pin1_4 | 418 | 423 | PF00397 | 0.728 |
LIG_14-3-3_CanoR_1 | 258 | 264 | PF00244 | 0.676 |
LIG_APCC_ABBA_1 | 343 | 348 | PF00400 | 0.334 |
LIG_APCC_ABBA_1 | 349 | 354 | PF00400 | 0.404 |
LIG_APCC_ABBA_1 | 71 | 76 | PF00400 | 0.420 |
LIG_BRCT_BRCA1_1 | 281 | 285 | PF00533 | 0.476 |
LIG_EH1_1 | 284 | 292 | PF00400 | 0.476 |
LIG_FHA_1 | 118 | 124 | PF00498 | 0.490 |
LIG_FHA_1 | 233 | 239 | PF00498 | 0.509 |
LIG_FHA_1 | 282 | 288 | PF00498 | 0.487 |
LIG_FHA_1 | 318 | 324 | PF00498 | 0.476 |
LIG_FHA_1 | 336 | 342 | PF00498 | 0.492 |
LIG_FHA_1 | 384 | 390 | PF00498 | 0.520 |
LIG_FHA_1 | 62 | 68 | PF00498 | 0.364 |
LIG_FHA_2 | 145 | 151 | PF00498 | 0.716 |
LIG_FHA_2 | 201 | 207 | PF00498 | 0.412 |
LIG_FHA_2 | 361 | 367 | PF00498 | 0.410 |
LIG_FHA_2 | 37 | 43 | PF00498 | 0.450 |
LIG_FHA_2 | 426 | 432 | PF00498 | 0.532 |
LIG_LIR_Apic_2 | 435 | 440 | PF02991 | 0.669 |
LIG_LIR_Gen_1 | 64 | 73 | PF02991 | 0.388 |
LIG_LIR_Nem_3 | 64 | 68 | PF02991 | 0.345 |
LIG_MYND_1 | 17 | 21 | PF01753 | 0.437 |
LIG_RPA_C_Fungi | 294 | 306 | PF08784 | 0.323 |
LIG_SH2_PTP2 | 217 | 220 | PF00017 | 0.346 |
LIG_SH2_SRC | 178 | 181 | PF00017 | 0.597 |
LIG_SH2_STAP1 | 312 | 316 | PF00017 | 0.346 |
LIG_SH2_STAT5 | 18 | 21 | PF00017 | 0.440 |
LIG_SH2_STAT5 | 217 | 220 | PF00017 | 0.346 |
LIG_SH3_1 | 18 | 24 | PF00018 | 0.438 |
LIG_SH3_3 | 136 | 142 | PF00018 | 0.751 |
LIG_SH3_3 | 18 | 24 | PF00018 | 0.501 |
LIG_SH3_3 | 269 | 275 | PF00018 | 0.698 |
LIG_SH3_3 | 420 | 426 | PF00018 | 0.618 |
LIG_SUMO_SIM_anti_2 | 10 | 17 | PF11976 | 0.424 |
LIG_SUMO_SIM_anti_2 | 286 | 291 | PF11976 | 0.314 |
LIG_TRAF2_1 | 196 | 199 | PF00917 | 0.475 |
MOD_CK1_1 | 122 | 128 | PF00069 | 0.562 |
MOD_CK1_1 | 144 | 150 | PF00069 | 0.649 |
MOD_CK1_1 | 193 | 199 | PF00069 | 0.551 |
MOD_CK1_1 | 240 | 246 | PF00069 | 0.530 |
MOD_CK1_1 | 256 | 262 | PF00069 | 0.769 |
MOD_CK1_1 | 268 | 274 | PF00069 | 0.597 |
MOD_CK1_1 | 360 | 366 | PF00069 | 0.577 |
MOD_CK1_1 | 384 | 390 | PF00069 | 0.632 |
MOD_CK2_1 | 164 | 170 | PF00069 | 0.617 |
MOD_CK2_1 | 193 | 199 | PF00069 | 0.473 |
MOD_CK2_1 | 200 | 206 | PF00069 | 0.400 |
MOD_CK2_1 | 36 | 42 | PF00069 | 0.437 |
MOD_CK2_1 | 360 | 366 | PF00069 | 0.408 |
MOD_CK2_1 | 425 | 431 | PF00069 | 0.646 |
MOD_GlcNHglycan | 134 | 137 | PF01048 | 0.493 |
MOD_GlcNHglycan | 167 | 170 | PF01048 | 0.606 |
MOD_GlcNHglycan | 193 | 196 | PF01048 | 0.571 |
MOD_GlcNHglycan | 239 | 242 | PF01048 | 0.522 |
MOD_GlcNHglycan | 32 | 35 | PF01048 | 0.329 |
MOD_GlcNHglycan | 399 | 402 | PF01048 | 0.573 |
MOD_GlcNHglycan | 418 | 421 | PF01048 | 0.690 |
MOD_GSK3_1 | 117 | 124 | PF00069 | 0.621 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.642 |
MOD_GSK3_1 | 271 | 278 | PF00069 | 0.570 |
MOD_GSK3_1 | 38 | 45 | PF00069 | 0.446 |
MOD_GSK3_1 | 381 | 388 | PF00069 | 0.608 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.409 |
MOD_N-GLC_1 | 384 | 389 | PF02516 | 0.541 |
MOD_NEK2_1 | 107 | 112 | PF00069 | 0.619 |
MOD_NEK2_1 | 118 | 123 | PF00069 | 0.585 |
MOD_NEK2_1 | 132 | 137 | PF00069 | 0.499 |
MOD_NEK2_1 | 245 | 250 | PF00069 | 0.603 |
MOD_NEK2_1 | 263 | 268 | PF00069 | 0.508 |
MOD_NEK2_1 | 30 | 35 | PF00069 | 0.321 |
MOD_NEK2_1 | 357 | 362 | PF00069 | 0.467 |
MOD_NEK2_1 | 445 | 450 | PF00069 | 0.480 |
MOD_OFUCOSY | 251 | 257 | PF10250 | 0.524 |
MOD_OFUCOSY | 374 | 379 | PF10250 | 0.387 |
MOD_PIKK_1 | 178 | 184 | PF00454 | 0.594 |
MOD_PIKK_1 | 193 | 199 | PF00454 | 0.479 |
MOD_PIKK_1 | 450 | 456 | PF00454 | 0.617 |
MOD_PKA_1 | 375 | 381 | PF00069 | 0.438 |
MOD_PKA_1 | 84 | 90 | PF00069 | 0.524 |
MOD_PKA_2 | 107 | 113 | PF00069 | 0.501 |
MOD_PKA_2 | 374 | 380 | PF00069 | 0.502 |
MOD_PKA_2 | 84 | 90 | PF00069 | 0.618 |
MOD_Plk_1 | 384 | 390 | PF00069 | 0.542 |
MOD_Plk_2-3 | 42 | 48 | PF00069 | 0.447 |
MOD_Plk_4 | 141 | 147 | PF00069 | 0.508 |
MOD_Plk_4 | 432 | 438 | PF00069 | 0.595 |
MOD_Plk_4 | 52 | 58 | PF00069 | 0.401 |
MOD_Plk_4 | 61 | 67 | PF00069 | 0.372 |
MOD_ProDKin_1 | 246 | 252 | PF00069 | 0.593 |
MOD_ProDKin_1 | 256 | 262 | PF00069 | 0.673 |
MOD_ProDKin_1 | 268 | 274 | PF00069 | 0.574 |
MOD_ProDKin_1 | 418 | 424 | PF00069 | 0.731 |
TRG_DiLeu_BaEn_1 | 4 | 9 | PF01217 | 0.436 |
TRG_DiLeu_LyEn_5 | 170 | 175 | PF01217 | 0.435 |
TRG_ENDOCYTIC_2 | 217 | 220 | PF00928 | 0.346 |
TRG_ER_diArg_1 | 105 | 108 | PF00400 | 0.517 |
TRG_ER_diArg_1 | 209 | 211 | PF00400 | 0.384 |
TRG_ER_diArg_1 | 296 | 299 | PF00400 | 0.314 |
TRG_ER_diArg_1 | 84 | 86 | PF00400 | 0.634 |
TRG_Pf-PMV_PEXEL_1 | 299 | 303 | PF00026 | 0.314 |
TRG_Pf-PMV_PEXEL_1 | 307 | 311 | PF00026 | 0.314 |
TRG_Pf-PMV_PEXEL_1 | 359 | 364 | PF00026 | 0.474 |
TRG_Pf-PMV_PEXEL_1 | 84 | 89 | PF00026 | 0.523 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4Y0 | Leptomonas seymouri | 40% | 100% |
A0A3S7WX61 | Leishmania donovani | 68% | 92% |
A4HZT7 | Leishmania infantum | 68% | 92% |
E9AVP2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 69% | 92% |
Q4QBT7 | Leishmania major | 67% | 100% |