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: A4HKM1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 134 | 138 | PF00656 | 0.526 |
CLV_C14_Caspase3-7 | 251 | 255 | PF00656 | 0.725 |
CLV_NRD_NRD_1 | 210 | 212 | PF00675 | 0.587 |
CLV_NRD_NRD_1 | 34 | 36 | PF00675 | 0.654 |
CLV_NRD_NRD_1 | 439 | 441 | PF00675 | 0.663 |
CLV_NRD_NRD_1 | 71 | 73 | PF00675 | 0.463 |
CLV_NRD_NRD_1 | 96 | 98 | PF00675 | 0.661 |
CLV_PCSK_KEX2_1 | 210 | 212 | PF00082 | 0.587 |
CLV_PCSK_KEX2_1 | 263 | 265 | PF00082 | 0.823 |
CLV_PCSK_KEX2_1 | 34 | 36 | PF00082 | 0.654 |
CLV_PCSK_KEX2_1 | 362 | 364 | PF00082 | 0.797 |
CLV_PCSK_KEX2_1 | 439 | 441 | PF00082 | 0.663 |
CLV_PCSK_KEX2_1 | 71 | 73 | PF00082 | 0.489 |
CLV_PCSK_KEX2_1 | 96 | 98 | PF00082 | 0.661 |
CLV_PCSK_PC1ET2_1 | 263 | 265 | PF00082 | 0.823 |
CLV_PCSK_PC1ET2_1 | 362 | 364 | PF00082 | 0.797 |
CLV_PCSK_PC7_1 | 30 | 36 | PF00082 | 0.648 |
CLV_PCSK_SKI1_1 | 172 | 176 | PF00082 | 0.427 |
CLV_PCSK_SKI1_1 | 348 | 352 | PF00082 | 0.773 |
CLV_PCSK_SKI1_1 | 96 | 100 | PF00082 | 0.647 |
DEG_APCC_DBOX_1 | 118 | 126 | PF00400 | 0.515 |
DEG_ODPH_VHL_1 | 186 | 197 | PF01847 | 0.528 |
DOC_MAPK_gen_1 | 117 | 124 | PF00069 | 0.517 |
DOC_MAPK_gen_1 | 172 | 180 | PF00069 | 0.675 |
DOC_MAPK_gen_1 | 412 | 421 | PF00069 | 0.824 |
DOC_MAPK_MEF2A_6 | 414 | 423 | PF00069 | 0.558 |
DOC_PP1_RVXF_1 | 261 | 268 | PF00149 | 0.822 |
DOC_PP2B_LxvP_1 | 189 | 192 | PF13499 | 0.519 |
DOC_PP4_FxxP_1 | 123 | 126 | PF00568 | 0.515 |
DOC_USP7_MATH_1 | 346 | 350 | PF00917 | 0.782 |
DOC_USP7_MATH_1 | 82 | 86 | PF00917 | 0.533 |
DOC_WW_Pin1_4 | 255 | 260 | PF00397 | 0.838 |
DOC_WW_Pin1_4 | 294 | 299 | PF00397 | 0.588 |
DOC_WW_Pin1_4 | 373 | 378 | PF00397 | 0.840 |
LIG_14-3-3_CanoR_1 | 230 | 239 | PF00244 | 0.571 |
LIG_14-3-3_CanoR_1 | 275 | 280 | PF00244 | 0.547 |
LIG_14-3-3_CanoR_1 | 286 | 294 | PF00244 | 0.700 |
LIG_14-3-3_CanoR_1 | 348 | 353 | PF00244 | 0.773 |
LIG_14-3-3_CanoR_1 | 363 | 372 | PF00244 | 0.558 |
LIG_14-3-3_CanoR_1 | 414 | 420 | PF00244 | 0.556 |
LIG_14-3-3_CanoR_1 | 439 | 443 | PF00244 | 0.728 |
LIG_14-3-3_CanoR_1 | 447 | 452 | PF00244 | 0.606 |
LIG_Actin_WH2_1 | 412 | 427 | PF00022 | 0.560 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.529 |
LIG_BRCT_BRCA1_1 | 140 | 144 | PF00533 | 0.552 |
LIG_BRCT_BRCA1_1 | 337 | 341 | PF00533 | 0.723 |
LIG_FHA_1 | 144 | 150 | PF00498 | 0.534 |
LIG_FHA_1 | 173 | 179 | PF00498 | 0.574 |
LIG_FHA_1 | 181 | 187 | PF00498 | 0.499 |
LIG_FHA_1 | 192 | 198 | PF00498 | 0.535 |
LIG_FHA_1 | 217 | 223 | PF00498 | 0.532 |
LIG_FHA_1 | 34 | 40 | PF00498 | 0.654 |
LIG_FHA_1 | 340 | 346 | PF00498 | 0.830 |
LIG_FHA_1 | 389 | 395 | PF00498 | 0.541 |
LIG_FHA_1 | 399 | 405 | PF00498 | 0.516 |
LIG_FHA_2 | 132 | 138 | PF00498 | 0.524 |
LIG_FHA_2 | 196 | 202 | PF00498 | 0.583 |
LIG_FHA_2 | 23 | 29 | PF00498 | 0.641 |
LIG_LIR_Apic_2 | 121 | 126 | PF02991 | 0.518 |
LIG_LIR_Gen_1 | 271 | 281 | PF02991 | 0.643 |
LIG_LIR_Gen_1 | 9 | 18 | PF02991 | 0.416 |
LIG_LIR_Nem_3 | 271 | 276 | PF02991 | 0.789 |
LIG_LIR_Nem_3 | 9 | 15 | PF02991 | 0.653 |
LIG_SH2_GRB2like | 408 | 411 | PF00017 | 0.719 |
LIG_SH2_STAT5 | 106 | 109 | PF00017 | 0.421 |
LIG_SH2_STAT5 | 408 | 411 | PF00017 | 0.698 |
LIG_SH3_3 | 182 | 188 | PF00018 | 0.623 |
LIG_SH3_3 | 233 | 239 | PF00018 | 0.708 |
LIG_SH3_3 | 303 | 309 | PF00018 | 0.709 |
LIG_SH3_3 | 416 | 422 | PF00018 | 0.564 |
LIG_SUMO_SIM_par_1 | 166 | 171 | PF11976 | 0.471 |
LIG_SUMO_SIM_par_1 | 193 | 201 | PF11976 | 0.778 |
LIG_TRAF2_1 | 198 | 201 | PF00917 | 0.585 |
LIG_TRAF2_1 | 55 | 58 | PF00917 | 0.386 |
LIG_TRAF2_1 | 7 | 10 | PF00917 | 0.653 |
LIG_TRAF2_1 | 88 | 91 | PF00917 | 0.644 |
LIG_UBA3_1 | 122 | 128 | PF00899 | 0.517 |
LIG_UBA3_1 | 166 | 173 | PF00899 | 0.667 |
MOD_CDC14_SPxK_1 | 376 | 379 | PF00782 | 0.848 |
MOD_CDK_SPxK_1 | 373 | 379 | PF00069 | 0.842 |
MOD_CDK_SPxxK_3 | 255 | 262 | PF00069 | 0.737 |
MOD_CK1_1 | 127 | 133 | PF00069 | 0.659 |
MOD_CK1_1 | 193 | 199 | PF00069 | 0.605 |
MOD_CK1_1 | 218 | 224 | PF00069 | 0.673 |
MOD_CK1_1 | 297 | 303 | PF00069 | 0.570 |
MOD_CK1_1 | 390 | 396 | PF00069 | 0.580 |
MOD_CK1_1 | 426 | 432 | PF00069 | 0.785 |
MOD_CK1_1 | 435 | 441 | PF00069 | 0.540 |
MOD_CK2_1 | 195 | 201 | PF00069 | 0.707 |
MOD_CK2_1 | 255 | 261 | PF00069 | 0.739 |
MOD_CK2_1 | 268 | 274 | PF00069 | 0.545 |
MOD_CK2_1 | 3 | 9 | PF00069 | 0.674 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.699 |
MOD_GlcNHglycan | 212 | 215 | PF01048 | 0.564 |
MOD_GlcNHglycan | 240 | 243 | PF01048 | 0.589 |
MOD_GlcNHglycan | 250 | 253 | PF01048 | 0.554 |
MOD_GlcNHglycan | 309 | 312 | PF01048 | 0.710 |
MOD_GlcNHglycan | 327 | 330 | PF01048 | 0.549 |
MOD_GlcNHglycan | 337 | 340 | PF01048 | 0.734 |
MOD_GlcNHglycan | 348 | 351 | PF01048 | 0.647 |
MOD_GlcNHglycan | 425 | 428 | PF01048 | 0.845 |
MOD_GlcNHglycan | 6 | 9 | PF01048 | 0.665 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.528 |
MOD_GSK3_1 | 127 | 134 | PF00069 | 0.782 |
MOD_GSK3_1 | 136 | 143 | PF00069 | 0.643 |
MOD_GSK3_1 | 168 | 175 | PF00069 | 0.440 |
MOD_GSK3_1 | 191 | 198 | PF00069 | 0.708 |
MOD_GSK3_1 | 218 | 225 | PF00069 | 0.717 |
MOD_GSK3_1 | 327 | 334 | PF00069 | 0.695 |
MOD_GSK3_1 | 335 | 342 | PF00069 | 0.712 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.529 |
MOD_GSK3_1 | 434 | 441 | PF00069 | 0.727 |
MOD_GSK3_1 | 443 | 450 | PF00069 | 0.608 |
MOD_N-GLC_1 | 398 | 403 | PF02516 | 0.544 |
MOD_NEK2_1 | 166 | 171 | PF00069 | 0.447 |
MOD_NEK2_2 | 339 | 344 | PF00069 | 0.833 |
MOD_OFUCOSY | 325 | 331 | PF10250 | 0.568 |
MOD_PIKK_1 | 286 | 292 | PF00454 | 0.596 |
MOD_PIKK_1 | 331 | 337 | PF00454 | 0.789 |
MOD_PIKK_1 | 370 | 376 | PF00454 | 0.727 |
MOD_PIKK_1 | 426 | 432 | PF00454 | 0.579 |
MOD_PIKK_1 | 62 | 68 | PF00454 | 0.543 |
MOD_PKA_1 | 172 | 178 | PF00069 | 0.418 |
MOD_PKA_1 | 210 | 216 | PF00069 | 0.571 |
MOD_PKA_2 | 210 | 216 | PF00069 | 0.839 |
MOD_PKA_2 | 229 | 235 | PF00069 | 0.517 |
MOD_PKA_2 | 237 | 243 | PF00069 | 0.562 |
MOD_PKA_2 | 274 | 280 | PF00069 | 0.814 |
MOD_PKA_2 | 285 | 291 | PF00069 | 0.861 |
MOD_PKA_2 | 33 | 39 | PF00069 | 0.652 |
MOD_PKA_2 | 335 | 341 | PF00069 | 0.682 |
MOD_PKA_2 | 364 | 370 | PF00069 | 0.799 |
MOD_PKA_2 | 435 | 441 | PF00069 | 0.748 |
MOD_PKA_2 | 446 | 452 | PF00069 | 0.604 |
MOD_PKA_2 | 82 | 88 | PF00069 | 0.651 |
MOD_Plk_1 | 153 | 159 | PF00069 | 0.686 |
MOD_Plk_4 | 127 | 133 | PF00069 | 0.514 |
MOD_Plk_4 | 153 | 159 | PF00069 | 0.761 |
MOD_Plk_4 | 218 | 224 | PF00069 | 0.740 |
MOD_Plk_4 | 348 | 354 | PF00069 | 0.771 |
MOD_ProDKin_1 | 255 | 261 | PF00069 | 0.837 |
MOD_ProDKin_1 | 294 | 300 | PF00069 | 0.587 |
MOD_ProDKin_1 | 373 | 379 | PF00069 | 0.842 |
MOD_SUMO_rev_2 | 258 | 265 | PF00179 | 0.805 |
TRG_DiLeu_BaEn_1 | 10 | 15 | PF01217 | 0.651 |
TRG_DiLeu_BaEn_2 | 94 | 100 | PF01217 | 0.380 |
TRG_DiLeu_BaLyEn_6 | 419 | 424 | PF01217 | 0.564 |
TRG_ENDOCYTIC_2 | 12 | 15 | PF00928 | 0.653 |
TRG_ER_diArg_1 | 117 | 120 | PF00400 | 0.738 |
TRG_ER_diArg_1 | 210 | 212 | PF00400 | 0.587 |
TRG_ER_diArg_1 | 71 | 73 | PF00400 | 0.451 |
TRG_Pf-PMV_PEXEL_1 | 71 | 75 | PF00026 | 0.550 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8ITE5 | Leishmania donovani | 61% | 100% |
A4I853 | Leishmania infantum | 62% | 100% |
E9B310 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 63% | 100% |
Q4Q545 | Leishmania major | 63% | 100% |