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: 1, no: 5 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: Q4QD02
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 7 |
GO:0005488 | binding | 1 | 7 |
GO:0016787 | hydrolase activity | 2 | 7 |
GO:0043167 | ion binding | 2 | 7 |
GO:0043169 | cation binding | 3 | 7 |
GO:0046872 | metal ion binding | 4 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 155 | 159 | PF00656 | 0.537 |
CLV_C14_Caspase3-7 | 398 | 402 | PF00656 | 0.734 |
CLV_NRD_NRD_1 | 138 | 140 | PF00675 | 0.602 |
CLV_NRD_NRD_1 | 277 | 279 | PF00675 | 0.495 |
CLV_NRD_NRD_1 | 350 | 352 | PF00675 | 0.613 |
CLV_PCSK_KEX2_1 | 138 | 140 | PF00082 | 0.602 |
CLV_PCSK_KEX2_1 | 277 | 279 | PF00082 | 0.517 |
CLV_PCSK_KEX2_1 | 350 | 352 | PF00082 | 0.613 |
CLV_PCSK_KEX2_1 | 50 | 52 | PF00082 | 0.470 |
CLV_PCSK_PC1ET2_1 | 50 | 52 | PF00082 | 0.492 |
CLV_PCSK_SKI1_1 | 173 | 177 | PF00082 | 0.742 |
CLV_PCSK_SKI1_1 | 31 | 35 | PF00082 | 0.696 |
CLV_PCSK_SKI1_1 | 351 | 355 | PF00082 | 0.517 |
CLV_PCSK_SKI1_1 | 95 | 99 | PF00082 | 0.740 |
DEG_ODPH_VHL_1 | 288 | 301 | PF01847 | 0.577 |
DOC_MAPK_gen_1 | 54 | 63 | PF00069 | 0.441 |
DOC_MAPK_MEF2A_6 | 385 | 392 | PF00069 | 0.529 |
DOC_MAPK_MEF2A_6 | 40 | 48 | PF00069 | 0.579 |
DOC_MAPK_MEF2A_6 | 54 | 63 | PF00069 | 0.415 |
DOC_PP2B_LxvP_1 | 288 | 291 | PF13499 | 0.488 |
DOC_PP4_FxxP_1 | 355 | 358 | PF00568 | 0.580 |
DOC_USP7_MATH_1 | 169 | 173 | PF00917 | 0.722 |
DOC_USP7_MATH_1 | 184 | 188 | PF00917 | 0.408 |
DOC_USP7_MATH_1 | 198 | 202 | PF00917 | 0.439 |
DOC_USP7_MATH_1 | 217 | 221 | PF00917 | 0.478 |
DOC_USP7_MATH_1 | 331 | 335 | PF00917 | 0.725 |
DOC_USP7_UBL2_3 | 50 | 54 | PF12436 | 0.519 |
DOC_WW_Pin1_4 | 194 | 199 | PF00397 | 0.528 |
DOC_WW_Pin1_4 | 268 | 273 | PF00397 | 0.429 |
DOC_WW_Pin1_4 | 315 | 320 | PF00397 | 0.744 |
LIG_14-3-3_CanoR_1 | 11 | 17 | PF00244 | 0.478 |
LIG_14-3-3_CanoR_1 | 173 | 178 | PF00244 | 0.552 |
LIG_Actin_WH2_2 | 176 | 192 | PF00022 | 0.519 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.523 |
LIG_BRCT_BRCA1_1 | 282 | 286 | PF00533 | 0.546 |
LIG_deltaCOP1_diTrp_1 | 146 | 152 | PF00928 | 0.539 |
LIG_eIF4E_1 | 208 | 214 | PF01652 | 0.452 |
LIG_FHA_1 | 13 | 19 | PF00498 | 0.396 |
LIG_FHA_1 | 165 | 171 | PF00498 | 0.675 |
LIG_FHA_1 | 290 | 296 | PF00498 | 0.473 |
LIG_FHA_1 | 4 | 10 | PF00498 | 0.566 |
LIG_FHA_1 | 76 | 82 | PF00498 | 0.551 |
LIG_FHA_2 | 342 | 348 | PF00498 | 0.738 |
LIG_FHA_2 | 396 | 402 | PF00498 | 0.726 |
LIG_FHA_2 | 96 | 102 | PF00498 | 0.691 |
LIG_IRF3_LxIS_1 | 264 | 271 | PF10401 | 0.352 |
LIG_LIR_Apic_2 | 266 | 272 | PF02991 | 0.477 |
LIG_LIR_Apic_2 | 371 | 377 | PF02991 | 0.632 |
LIG_LIR_Gen_1 | 207 | 218 | PF02991 | 0.478 |
LIG_LIR_Gen_1 | 292 | 301 | PF02991 | 0.469 |
LIG_LIR_Gen_1 | 304 | 313 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 207 | 213 | PF02991 | 0.392 |
LIG_LIR_Nem_3 | 292 | 296 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 304 | 308 | PF02991 | 0.471 |
LIG_MYND_3 | 255 | 259 | PF01753 | 0.621 |
LIG_Pex14_2 | 387 | 391 | PF04695 | 0.679 |
LIG_Rb_LxCxE_1 | 333 | 348 | PF01857 | 0.623 |
LIG_SH2_CRK | 181 | 185 | PF00017 | 0.426 |
LIG_SH2_CRK | 210 | 214 | PF00017 | 0.394 |
LIG_SH2_NCK_1 | 181 | 185 | PF00017 | 0.426 |
LIG_SH2_NCK_1 | 74 | 78 | PF00017 | 0.485 |
LIG_SH2_PTP2 | 62 | 65 | PF00017 | 0.458 |
LIG_SH2_STAP1 | 205 | 209 | PF00017 | 0.424 |
LIG_SH2_STAP1 | 210 | 214 | PF00017 | 0.387 |
LIG_SH2_STAT5 | 208 | 211 | PF00017 | 0.429 |
LIG_SH2_STAT5 | 293 | 296 | PF00017 | 0.562 |
LIG_SH2_STAT5 | 361 | 364 | PF00017 | 0.552 |
LIG_SH2_STAT5 | 374 | 377 | PF00017 | 0.357 |
LIG_SH2_STAT5 | 62 | 65 | PF00017 | 0.458 |
LIG_SH2_STAT5 | 80 | 83 | PF00017 | 0.511 |
LIG_SH3_3 | 313 | 319 | PF00018 | 0.718 |
LIG_SH3_3 | 4 | 10 | PF00018 | 0.514 |
LIG_SUMO_SIM_anti_2 | 14 | 20 | PF11976 | 0.458 |
LIG_TRAF2_1 | 110 | 113 | PF00917 | 0.611 |
LIG_TRAF2_1 | 251 | 254 | PF00917 | 0.670 |
LIG_TRFH_1 | 286 | 290 | PF08558 | 0.491 |
LIG_WW_1 | 290 | 293 | PF00397 | 0.585 |
MOD_CDK_SPK_2 | 194 | 199 | PF00069 | 0.535 |
MOD_CK1_1 | 262 | 268 | PF00069 | 0.519 |
MOD_CK1_1 | 304 | 310 | PF00069 | 0.467 |
MOD_CK1_1 | 343 | 349 | PF00069 | 0.634 |
MOD_CK2_1 | 107 | 113 | PF00069 | 0.579 |
MOD_CK2_1 | 142 | 148 | PF00069 | 0.471 |
MOD_CK2_1 | 234 | 240 | PF00069 | 0.749 |
MOD_CK2_1 | 268 | 274 | PF00069 | 0.548 |
MOD_CK2_1 | 341 | 347 | PF00069 | 0.742 |
MOD_CK2_1 | 365 | 371 | PF00069 | 0.575 |
MOD_CMANNOS | 149 | 152 | PF00535 | 0.611 |
MOD_Cter_Amidation | 348 | 351 | PF01082 | 0.627 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.565 |
MOD_GlcNHglycan | 109 | 112 | PF01048 | 0.699 |
MOD_GlcNHglycan | 215 | 218 | PF01048 | 0.623 |
MOD_GlcNHglycan | 219 | 222 | PF01048 | 0.663 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.734 |
MOD_GSK3_1 | 169 | 176 | PF00069 | 0.589 |
MOD_GSK3_1 | 194 | 201 | PF00069 | 0.467 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.388 |
MOD_GSK3_1 | 229 | 236 | PF00069 | 0.537 |
MOD_GSK3_1 | 280 | 287 | PF00069 | 0.509 |
MOD_GSK3_1 | 297 | 304 | PF00069 | 0.482 |
MOD_NEK2_1 | 102 | 107 | PF00069 | 0.694 |
MOD_NEK2_1 | 12 | 17 | PF00069 | 0.462 |
MOD_NEK2_1 | 213 | 218 | PF00069 | 0.600 |
MOD_NEK2_1 | 362 | 367 | PF00069 | 0.691 |
MOD_NEK2_2 | 185 | 190 | PF00069 | 0.592 |
MOD_OFUCOSY | 231 | 238 | PF10250 | 0.569 |
MOD_PIKK_1 | 230 | 236 | PF00454 | 0.762 |
MOD_PIKK_1 | 96 | 102 | PF00454 | 0.753 |
MOD_PKA_1 | 95 | 101 | PF00069 | 0.716 |
MOD_PKA_2 | 198 | 204 | PF00069 | 0.568 |
MOD_PKB_1 | 202 | 210 | PF00069 | 0.363 |
MOD_Plk_4 | 12 | 18 | PF00069 | 0.465 |
MOD_Plk_4 | 173 | 179 | PF00069 | 0.563 |
MOD_Plk_4 | 204 | 210 | PF00069 | 0.479 |
MOD_Plk_4 | 289 | 295 | PF00069 | 0.475 |
MOD_Plk_4 | 331 | 337 | PF00069 | 0.553 |
MOD_Plk_4 | 407 | 413 | PF00069 | 0.728 |
MOD_ProDKin_1 | 194 | 200 | PF00069 | 0.533 |
MOD_ProDKin_1 | 268 | 274 | PF00069 | 0.436 |
MOD_ProDKin_1 | 315 | 321 | PF00069 | 0.751 |
MOD_SUMO_rev_2 | 91 | 98 | PF00179 | 0.661 |
TRG_DiLeu_BaEn_1 | 263 | 268 | PF01217 | 0.505 |
TRG_DiLeu_BaLyEn_6 | 253 | 258 | PF01217 | 0.636 |
TRG_ENDOCYTIC_2 | 210 | 213 | PF00928 | 0.396 |
TRG_ENDOCYTIC_2 | 293 | 296 | PF00928 | 0.520 |
TRG_ER_diArg_1 | 137 | 139 | PF00400 | 0.577 |
TRG_ER_diArg_1 | 276 | 278 | PF00400 | 0.503 |
TRG_ER_diArg_1 | 350 | 352 | PF00400 | 0.671 |
TRG_Pf-PMV_PEXEL_1 | 127 | 131 | PF00026 | 0.463 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IIQ0 | Leptomonas seymouri | 50% | 100% |
A0A3S7WVU6 | Leishmania donovani | 93% | 100% |
A4HYN2 | Leishmania infantum | 93% | 100% |
E9AI97 | Leishmania braziliensis | 74% | 100% |
E9AUI2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |