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: A4HPS7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 56 | 60 | PF00656 | 0.774 |
CLV_MEL_PAP_1 | 4 | 10 | PF00089 | 0.506 |
CLV_NRD_NRD_1 | 133 | 135 | PF00675 | 0.551 |
CLV_NRD_NRD_1 | 384 | 386 | PF00675 | 0.509 |
CLV_NRD_NRD_1 | 390 | 392 | PF00675 | 0.543 |
CLV_NRD_NRD_1 | 85 | 87 | PF00675 | 0.495 |
CLV_PCSK_KEX2_1 | 133 | 135 | PF00082 | 0.626 |
CLV_PCSK_KEX2_1 | 281 | 283 | PF00082 | 0.803 |
CLV_PCSK_KEX2_1 | 384 | 386 | PF00082 | 0.602 |
CLV_PCSK_KEX2_1 | 390 | 392 | PF00082 | 0.670 |
CLV_PCSK_KEX2_1 | 85 | 87 | PF00082 | 0.495 |
CLV_PCSK_PC1ET2_1 | 281 | 283 | PF00082 | 0.803 |
CLV_PCSK_SKI1_1 | 113 | 117 | PF00082 | 0.581 |
CLV_PCSK_SKI1_1 | 29 | 33 | PF00082 | 0.730 |
CLV_PCSK_SKI1_1 | 413 | 417 | PF00082 | 0.581 |
DEG_MDM2_SWIB_1 | 158 | 165 | PF02201 | 0.591 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.777 |
DEG_SPOP_SBC_1 | 190 | 194 | PF00917 | 0.698 |
DEG_SPOP_SBC_1 | 329 | 333 | PF00917 | 0.576 |
DOC_CYCLIN_yCln2_LP_2 | 135 | 141 | PF00134 | 0.640 |
DOC_CYCLIN_yCln2_LP_2 | 31 | 34 | PF00134 | 0.723 |
DOC_MAPK_gen_1 | 381 | 389 | PF00069 | 0.426 |
DOC_PP2B_LxvP_1 | 135 | 138 | PF13499 | 0.642 |
DOC_PP2B_LxvP_1 | 219 | 222 | PF13499 | 0.593 |
DOC_PP2B_LxvP_1 | 266 | 269 | PF13499 | 0.788 |
DOC_PP2B_LxvP_1 | 31 | 34 | PF13499 | 0.723 |
DOC_PP2B_LxvP_1 | 55 | 58 | PF13499 | 0.520 |
DOC_PP4_FxxP_1 | 8 | 11 | PF00568 | 0.496 |
DOC_USP7_MATH_1 | 120 | 124 | PF00917 | 0.636 |
DOC_USP7_MATH_1 | 126 | 130 | PF00917 | 0.525 |
DOC_USP7_MATH_1 | 139 | 143 | PF00917 | 0.320 |
DOC_USP7_MATH_1 | 228 | 232 | PF00917 | 0.592 |
DOC_USP7_MATH_1 | 260 | 264 | PF00917 | 0.542 |
DOC_USP7_MATH_1 | 342 | 346 | PF00917 | 0.770 |
DOC_USP7_MATH_1 | 396 | 400 | PF00917 | 0.430 |
DOC_USP7_MATH_1 | 51 | 55 | PF00917 | 0.757 |
DOC_WW_Pin1_4 | 32 | 37 | PF00397 | 0.690 |
DOC_WW_Pin1_4 | 330 | 335 | PF00397 | 0.578 |
LIG_14-3-3_CanoR_1 | 113 | 122 | PF00244 | 0.588 |
LIG_14-3-3_CanoR_1 | 2 | 11 | PF00244 | 0.625 |
LIG_14-3-3_CanoR_1 | 202 | 209 | PF00244 | 0.626 |
LIG_14-3-3_CanoR_1 | 229 | 233 | PF00244 | 0.694 |
LIG_14-3-3_CanoR_1 | 86 | 92 | PF00244 | 0.529 |
LIG_BRCT_BRCA1_1 | 154 | 158 | PF00533 | 0.591 |
LIG_BRCT_BRCA1_1 | 230 | 234 | PF00533 | 0.588 |
LIG_BRCT_BRCA1_1 | 4 | 8 | PF00533 | 0.505 |
LIG_Clathr_ClatBox_1 | 415 | 419 | PF01394 | 0.440 |
LIG_EVH1_2 | 68 | 72 | PF00568 | 0.743 |
LIG_FHA_1 | 114 | 120 | PF00498 | 0.626 |
LIG_FHA_1 | 263 | 269 | PF00498 | 0.540 |
LIG_FHA_1 | 366 | 372 | PF00498 | 0.553 |
LIG_FHA_2 | 184 | 190 | PF00498 | 0.639 |
LIG_FHA_2 | 54 | 60 | PF00498 | 0.771 |
LIG_LIR_Apic_2 | 5 | 11 | PF02991 | 0.504 |
LIG_LIR_Gen_1 | 155 | 166 | PF02991 | 0.594 |
LIG_LIR_Nem_3 | 155 | 161 | PF02991 | 0.587 |
LIG_NRBOX | 40 | 46 | PF00104 | 0.668 |
LIG_PCNA_yPIPBox_3 | 402 | 416 | PF02747 | 0.659 |
LIG_Pex14_2 | 127 | 131 | PF04695 | 0.613 |
LIG_Pex14_2 | 154 | 158 | PF04695 | 0.591 |
LIG_SH2_STAT3 | 149 | 152 | PF00017 | 0.471 |
LIG_SH2_STAT5 | 160 | 163 | PF00017 | 0.423 |
LIG_SH2_STAT5 | 404 | 407 | PF00017 | 0.661 |
LIG_SH3_3 | 116 | 122 | PF00018 | 0.638 |
LIG_SH3_3 | 212 | 218 | PF00018 | 0.723 |
LIG_SH3_3 | 254 | 260 | PF00018 | 0.580 |
LIG_SH3_3 | 30 | 36 | PF00018 | 0.705 |
LIG_SH3_3 | 315 | 321 | PF00018 | 0.657 |
LIG_Sin3_3 | 301 | 308 | PF02671 | 0.524 |
LIG_SUMO_SIM_anti_2 | 39 | 45 | PF11976 | 0.413 |
LIG_SUMO_SIM_par_1 | 367 | 372 | PF11976 | 0.705 |
LIG_SUMO_SIM_par_1 | 41 | 48 | PF11976 | 0.405 |
LIG_SUMO_SIM_par_1 | 414 | 420 | PF11976 | 0.440 |
LIG_WRC_WIRS_1 | 405 | 410 | PF05994 | 0.400 |
MOD_CDK_SPK_2 | 330 | 335 | PF00069 | 0.578 |
MOD_CK1_1 | 346 | 352 | PF00069 | 0.726 |
MOD_CK1_1 | 355 | 361 | PF00069 | 0.618 |
MOD_CK1_1 | 6 | 12 | PF00069 | 0.744 |
MOD_CK1_1 | 73 | 79 | PF00069 | 0.618 |
MOD_CK2_1 | 330 | 336 | PF00069 | 0.579 |
MOD_CK2_1 | 411 | 417 | PF00069 | 0.563 |
MOD_Cter_Amidation | 279 | 282 | PF01082 | 0.808 |
MOD_GlcNHglycan | 116 | 119 | PF01048 | 0.376 |
MOD_GlcNHglycan | 19 | 22 | PF01048 | 0.492 |
MOD_GlcNHglycan | 204 | 207 | PF01048 | 0.811 |
MOD_GlcNHglycan | 247 | 250 | PF01048 | 0.637 |
MOD_GlcNHglycan | 262 | 265 | PF01048 | 0.604 |
MOD_GlcNHglycan | 288 | 291 | PF01048 | 0.721 |
MOD_GlcNHglycan | 294 | 297 | PF01048 | 0.793 |
MOD_GlcNHglycan | 345 | 348 | PF01048 | 0.654 |
MOD_GlcNHglycan | 357 | 360 | PF01048 | 0.567 |
MOD_GlcNHglycan | 47 | 50 | PF01048 | 0.709 |
MOD_GlcNHglycan | 72 | 75 | PF01048 | 0.715 |
MOD_GSK3_1 | 109 | 116 | PF00069 | 0.592 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.590 |
MOD_GSK3_1 | 198 | 205 | PF00069 | 0.638 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.690 |
MOD_GSK3_1 | 286 | 293 | PF00069 | 0.625 |
MOD_GSK3_1 | 342 | 349 | PF00069 | 0.599 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.616 |
MOD_N-GLC_1 | 27 | 32 | PF02516 | 0.471 |
MOD_N-GLC_1 | 343 | 348 | PF02516 | 0.580 |
MOD_NEK2_1 | 107 | 112 | PF00069 | 0.405 |
MOD_NEK2_1 | 114 | 119 | PF00069 | 0.479 |
MOD_NEK2_1 | 198 | 203 | PF00069 | 0.596 |
MOD_NEK2_1 | 292 | 297 | PF00069 | 0.723 |
MOD_NEK2_1 | 45 | 50 | PF00069 | 0.700 |
MOD_NEK2_2 | 139 | 144 | PF00069 | 0.631 |
MOD_NEK2_2 | 153 | 158 | PF00069 | 0.363 |
MOD_PIKK_1 | 228 | 234 | PF00454 | 0.588 |
MOD_PKA_2 | 228 | 234 | PF00069 | 0.588 |
MOD_PKA_2 | 45 | 51 | PF00069 | 0.476 |
MOD_PKA_2 | 6 | 12 | PF00069 | 0.506 |
MOD_Plk_1 | 27 | 33 | PF00069 | 0.501 |
MOD_Plk_1 | 343 | 349 | PF00069 | 0.581 |
MOD_Plk_4 | 153 | 159 | PF00069 | 0.553 |
MOD_Plk_4 | 262 | 268 | PF00069 | 0.545 |
MOD_Plk_4 | 95 | 101 | PF00069 | 0.616 |
MOD_ProDKin_1 | 32 | 38 | PF00069 | 0.681 |
MOD_ProDKin_1 | 330 | 336 | PF00069 | 0.579 |
TRG_DiLeu_BaEn_2 | 9 | 15 | PF01217 | 0.505 |
TRG_DiLeu_BaLyEn_6 | 167 | 172 | PF01217 | 0.694 |
TRG_ER_diArg_1 | 133 | 135 | PF00400 | 0.626 |
TRG_ER_diArg_1 | 383 | 385 | PF00400 | 0.595 |
TRG_ER_diArg_1 | 389 | 391 | PF00400 | 0.674 |
TRG_ER_diArg_1 | 85 | 87 | PF00400 | 0.623 |
TRG_Pf-PMV_PEXEL_1 | 381 | 386 | PF00026 | 0.488 |
TRG_Pf-PMV_PEXEL_1 | 413 | 417 | PF00026 | 0.413 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8ILA1 | Leishmania donovani | 69% | 99% |
A4IE65 | Leishmania infantum | 70% | 99% |
E9ATJ2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 67% | 99% |
Q4Q106 | Leishmania major | 68% | 100% |