Uncharacterized Protein, Uncharacterized
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: A4I7H9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 19 | 23 | PF00656 | 0.702 |
CLV_NRD_NRD_1 | 161 | 163 | PF00675 | 0.816 |
CLV_NRD_NRD_1 | 199 | 201 | PF00675 | 0.710 |
CLV_NRD_NRD_1 | 241 | 243 | PF00675 | 0.731 |
CLV_NRD_NRD_1 | 350 | 352 | PF00675 | 0.805 |
CLV_PCSK_FUR_1 | 197 | 201 | PF00082 | 0.709 |
CLV_PCSK_FUR_1 | 70 | 74 | PF00082 | 0.642 |
CLV_PCSK_KEX2_1 | 199 | 201 | PF00082 | 0.653 |
CLV_PCSK_KEX2_1 | 241 | 243 | PF00082 | 0.729 |
CLV_PCSK_KEX2_1 | 346 | 348 | PF00082 | 0.791 |
CLV_PCSK_KEX2_1 | 368 | 370 | PF00082 | 0.708 |
CLV_PCSK_KEX2_1 | 69 | 71 | PF00082 | 0.780 |
CLV_PCSK_KEX2_1 | 72 | 74 | PF00082 | 0.734 |
CLV_PCSK_KEX2_1 | 75 | 77 | PF00082 | 0.690 |
CLV_PCSK_KEX2_1 | 80 | 82 | PF00082 | 0.569 |
CLV_PCSK_PC1ET2_1 | 346 | 348 | PF00082 | 0.791 |
CLV_PCSK_PC1ET2_1 | 368 | 370 | PF00082 | 0.708 |
CLV_PCSK_PC1ET2_1 | 69 | 71 | PF00082 | 0.780 |
CLV_PCSK_PC1ET2_1 | 72 | 74 | PF00082 | 0.734 |
CLV_PCSK_PC1ET2_1 | 75 | 77 | PF00082 | 0.690 |
CLV_PCSK_PC1ET2_1 | 80 | 82 | PF00082 | 0.569 |
CLV_PCSK_PC7_1 | 76 | 82 | PF00082 | 0.793 |
CLV_PCSK_SKI1_1 | 337 | 341 | PF00082 | 0.707 |
CLV_PCSK_SKI1_1 | 372 | 376 | PF00082 | 0.679 |
CLV_PCSK_SKI1_1 | 66 | 70 | PF00082 | 0.731 |
CLV_PCSK_SKI1_1 | 72 | 76 | PF00082 | 0.555 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.745 |
DEG_SPOP_SBC_1 | 23 | 27 | PF00917 | 0.666 |
DEG_SPOP_SBC_1 | 305 | 309 | PF00917 | 0.542 |
DOC_ANK_TNKS_1 | 143 | 150 | PF00023 | 0.755 |
DOC_MAPK_gen_1 | 80 | 87 | PF00069 | 0.637 |
DOC_MAPK_MEF2A_6 | 171 | 179 | PF00069 | 0.726 |
DOC_MAPK_MEF2A_6 | 80 | 87 | PF00069 | 0.616 |
DOC_PP4_FxxP_1 | 331 | 334 | PF00568 | 0.780 |
DOC_USP7_MATH_1 | 138 | 142 | PF00917 | 0.809 |
DOC_USP7_MATH_1 | 23 | 27 | PF00917 | 0.688 |
DOC_USP7_MATH_1 | 277 | 281 | PF00917 | 0.741 |
DOC_USP7_MATH_1 | 339 | 343 | PF00917 | 0.705 |
DOC_USP7_MATH_1 | 83 | 87 | PF00917 | 0.736 |
DOC_USP7_UBL2_3 | 163 | 167 | PF12436 | 0.765 |
DOC_WW_Pin1_4 | 224 | 229 | PF00397 | 0.655 |
DOC_WW_Pin1_4 | 306 | 311 | PF00397 | 0.825 |
DOC_WW_Pin1_4 | 56 | 61 | PF00397 | 0.791 |
LIG_14-3-3_CanoR_1 | 101 | 108 | PF00244 | 0.557 |
LIG_14-3-3_CanoR_1 | 183 | 192 | PF00244 | 0.735 |
LIG_14-3-3_CanoR_1 | 84 | 88 | PF00244 | 0.653 |
LIG_deltaCOP1_diTrp_1 | 267 | 273 | PF00928 | 0.661 |
LIG_FHA_1 | 150 | 156 | PF00498 | 0.635 |
LIG_FHA_2 | 193 | 199 | PF00498 | 0.645 |
LIG_FHA_2 | 225 | 231 | PF00498 | 0.661 |
LIG_HP1_1 | 83 | 87 | PF01393 | 0.619 |
LIG_LIR_Nem_3 | 2 | 7 | PF02991 | 0.746 |
LIG_MYND_1 | 60 | 64 | PF01753 | 0.759 |
LIG_Pex14_1 | 269 | 273 | PF04695 | 0.662 |
LIG_PTAP_UEV_1 | 17 | 22 | PF05743 | 0.694 |
LIG_SH2_CRK | 202 | 206 | PF00017 | 0.704 |
LIG_SH2_NCK_1 | 274 | 278 | PF00017 | 0.752 |
LIG_SH2_SRC | 7 | 10 | PF00017 | 0.574 |
LIG_SH2_STAP1 | 274 | 278 | PF00017 | 0.565 |
LIG_SH2_STAT5 | 274 | 277 | PF00017 | 0.750 |
LIG_SH2_STAT5 | 4 | 7 | PF00017 | 0.750 |
LIG_SH3_2 | 64 | 69 | PF14604 | 0.707 |
LIG_SH3_3 | 105 | 111 | PF00018 | 0.737 |
LIG_SH3_3 | 11 | 17 | PF00018 | 0.775 |
LIG_SH3_3 | 205 | 211 | PF00018 | 0.733 |
LIG_SH3_3 | 54 | 60 | PF00018 | 0.660 |
LIG_SH3_3 | 61 | 67 | PF00018 | 0.666 |
LIG_SUMO_SIM_par_1 | 175 | 180 | PF11976 | 0.801 |
LIG_SUMO_SIM_par_1 | 7 | 13 | PF11976 | 0.580 |
LIG_TRAF2_1 | 10 | 13 | PF00917 | 0.771 |
LIG_WRC_WIRS_1 | 270 | 275 | PF05994 | 0.603 |
LIG_WRC_WIRS_1 | 340 | 345 | PF05994 | 0.781 |
LIG_WRPW_2 | 65 | 68 | PF00400 | 0.594 |
MOD_CDK_SPxxK_3 | 306 | 313 | PF00069 | 0.830 |
MOD_CK1_1 | 169 | 175 | PF00069 | 0.615 |
MOD_CK1_1 | 27 | 33 | PF00069 | 0.787 |
MOD_CK1_1 | 272 | 278 | PF00069 | 0.743 |
MOD_CK1_1 | 45 | 51 | PF00069 | 0.674 |
MOD_CK2_1 | 224 | 230 | PF00069 | 0.663 |
MOD_GlcNHglycan | 103 | 106 | PF01048 | 0.754 |
MOD_GlcNHglycan | 139 | 143 | PF01048 | 0.717 |
MOD_GlcNHglycan | 171 | 174 | PF01048 | 0.719 |
MOD_GlcNHglycan | 18 | 21 | PF01048 | 0.772 |
MOD_GlcNHglycan | 251 | 254 | PF01048 | 0.729 |
MOD_GlcNHglycan | 29 | 32 | PF01048 | 0.694 |
MOD_GlcNHglycan | 293 | 296 | PF01048 | 0.637 |
MOD_GlcNHglycan | 326 | 329 | PF01048 | 0.634 |
MOD_GlcNHglycan | 378 | 381 | PF01048 | 0.728 |
MOD_GlcNHglycan | 383 | 386 | PF01048 | 0.676 |
MOD_GlcNHglycan | 46 | 50 | PF01048 | 0.501 |
MOD_GSK3_1 | 110 | 117 | PF00069 | 0.784 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.727 |
MOD_GSK3_1 | 245 | 252 | PF00069 | 0.647 |
MOD_GSK3_1 | 268 | 275 | PF00069 | 0.716 |
MOD_GSK3_1 | 291 | 298 | PF00069 | 0.784 |
MOD_GSK3_1 | 320 | 327 | PF00069 | 0.663 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.611 |
MOD_LATS_1 | 99 | 105 | PF00433 | 0.746 |
MOD_N-GLC_1 | 222 | 227 | PF02516 | 0.805 |
MOD_NEK2_1 | 273 | 278 | PF00069 | 0.630 |
MOD_NEK2_1 | 312 | 317 | PF00069 | 0.834 |
MOD_NEK2_1 | 338 | 343 | PF00069 | 0.642 |
MOD_NEK2_1 | 357 | 362 | PF00069 | 0.583 |
MOD_NEK2_2 | 269 | 274 | PF00069 | 0.715 |
MOD_OFUCOSY | 191 | 196 | PF10250 | 0.617 |
MOD_PIKK_1 | 245 | 251 | PF00454 | 0.631 |
MOD_PIKK_1 | 357 | 363 | PF00454 | 0.829 |
MOD_PKA_2 | 244 | 250 | PF00069 | 0.824 |
MOD_PKA_2 | 312 | 318 | PF00069 | 0.831 |
MOD_PKA_2 | 35 | 41 | PF00069 | 0.765 |
MOD_PKA_2 | 364 | 370 | PF00069 | 0.758 |
MOD_PKA_2 | 83 | 89 | PF00069 | 0.667 |
MOD_Plk_1 | 222 | 228 | PF00069 | 0.725 |
MOD_Plk_4 | 123 | 129 | PF00069 | 0.816 |
MOD_Plk_4 | 269 | 275 | PF00069 | 0.592 |
MOD_Plk_4 | 295 | 301 | PF00069 | 0.808 |
MOD_Plk_4 | 320 | 326 | PF00069 | 0.801 |
MOD_ProDKin_1 | 224 | 230 | PF00069 | 0.660 |
MOD_ProDKin_1 | 306 | 312 | PF00069 | 0.827 |
MOD_ProDKin_1 | 56 | 62 | PF00069 | 0.789 |
MOD_SUMO_rev_2 | 252 | 262 | PF00179 | 0.670 |
MOD_SUMO_rev_2 | 341 | 348 | PF00179 | 0.716 |
TRG_ENDOCYTIC_2 | 202 | 205 | PF00928 | 0.701 |
TRG_ER_diArg_1 | 240 | 242 | PF00400 | 0.732 |
TRG_ER_diArg_1 | 33 | 36 | PF00400 | 0.764 |
TRG_NLS_MonoExtC_3 | 68 | 73 | PF00514 | 0.643 |
TRG_NLS_MonoExtN_4 | 66 | 73 | PF00514 | 0.711 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8ICV9 | Leishmania donovani | 98% | 100% |
A4HJZ6 | Leishmania braziliensis | 61% | 98% |
E9B2D6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 100% |
Q4Q5S0 | Leishmania major | 88% | 100% |