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: A4HJZ6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 142 | 146 | PF00656 | 0.546 |
CLV_NRD_NRD_1 | 156 | 158 | PF00675 | 0.827 |
CLV_NRD_NRD_1 | 234 | 236 | PF00675 | 0.726 |
CLV_NRD_NRD_1 | 305 | 307 | PF00675 | 0.686 |
CLV_NRD_NRD_1 | 342 | 344 | PF00675 | 0.809 |
CLV_PCSK_KEX2_1 | 158 | 160 | PF00082 | 0.589 |
CLV_PCSK_KEX2_1 | 234 | 236 | PF00082 | 0.711 |
CLV_PCSK_KEX2_1 | 240 | 242 | PF00082 | 0.622 |
CLV_PCSK_KEX2_1 | 305 | 307 | PF00082 | 0.686 |
CLV_PCSK_KEX2_1 | 338 | 340 | PF00082 | 0.794 |
CLV_PCSK_KEX2_1 | 47 | 49 | PF00082 | 0.547 |
CLV_PCSK_KEX2_1 | 69 | 71 | PF00082 | 0.783 |
CLV_PCSK_KEX2_1 | 75 | 77 | PF00082 | 0.679 |
CLV_PCSK_KEX2_1 | 80 | 82 | PF00082 | 0.563 |
CLV_PCSK_PC1ET2_1 | 158 | 160 | PF00082 | 0.561 |
CLV_PCSK_PC1ET2_1 | 240 | 242 | PF00082 | 0.552 |
CLV_PCSK_PC1ET2_1 | 338 | 340 | PF00082 | 0.794 |
CLV_PCSK_PC1ET2_1 | 47 | 49 | PF00082 | 0.547 |
CLV_PCSK_PC1ET2_1 | 69 | 71 | PF00082 | 0.783 |
CLV_PCSK_PC1ET2_1 | 75 | 77 | PF00082 | 0.679 |
CLV_PCSK_PC1ET2_1 | 80 | 82 | PF00082 | 0.563 |
CLV_PCSK_PC7_1 | 76 | 82 | PF00082 | 0.785 |
CLV_PCSK_SKI1_1 | 116 | 120 | PF00082 | 0.499 |
CLV_PCSK_SKI1_1 | 158 | 162 | PF00082 | 0.702 |
CLV_PCSK_SKI1_1 | 186 | 190 | PF00082 | 0.534 |
CLV_PCSK_SKI1_1 | 36 | 40 | PF00082 | 0.552 |
CLV_PCSK_SKI1_1 | 69 | 73 | PF00082 | 0.603 |
CLV_PCSK_SKI1_1 | 80 | 84 | PF00082 | 0.554 |
CLV_Separin_Metazoa | 231 | 235 | PF03568 | 0.576 |
DEG_APCC_DBOX_1 | 115 | 123 | PF00400 | 0.504 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.679 |
DEG_SPOP_SBC_1 | 260 | 264 | PF00917 | 0.447 |
DOC_CDC14_PxL_1 | 52 | 60 | PF14671 | 0.540 |
DOC_MAPK_gen_1 | 69 | 79 | PF00069 | 0.565 |
DOC_PP4_FxxP_1 | 323 | 326 | PF00568 | 0.766 |
DOC_USP7_MATH_1 | 118 | 122 | PF00917 | 0.508 |
DOC_USP7_MATH_1 | 260 | 264 | PF00917 | 0.562 |
DOC_USP7_MATH_1 | 269 | 273 | PF00917 | 0.755 |
DOC_USP7_MATH_1 | 296 | 300 | PF00917 | 0.660 |
DOC_USP7_MATH_1 | 42 | 46 | PF00917 | 0.540 |
DOC_USP7_MATH_1 | 54 | 58 | PF00917 | 0.615 |
DOC_USP7_MATH_1 | 99 | 103 | PF00917 | 0.544 |
DOC_USP7_UBL2_3 | 158 | 162 | PF12436 | 0.783 |
DOC_USP7_UBL2_3 | 222 | 226 | PF12436 | 0.592 |
DOC_WW_Pin1_4 | 161 | 166 | PF00397 | 0.556 |
DOC_WW_Pin1_4 | 201 | 206 | PF00397 | 0.540 |
DOC_WW_Pin1_4 | 298 | 303 | PF00397 | 0.812 |
DOC_WW_Pin1_4 | 56 | 61 | PF00397 | 0.780 |
LIG_14-3-3_CanoR_1 | 241 | 247 | PF00244 | 0.521 |
LIG_APCC_ABBAyCdc20_2 | 40 | 46 | PF00400 | 0.542 |
LIG_Clathr_ClatBox_1 | 179 | 183 | PF01394 | 0.533 |
LIG_deltaCOP1_diTrp_1 | 259 | 265 | PF00928 | 0.659 |
LIG_FHA_1 | 47 | 53 | PF00498 | 0.551 |
LIG_FHA_2 | 288 | 294 | PF00498 | 0.523 |
LIG_LIR_Apic_2 | 322 | 326 | PF02991 | 0.516 |
LIG_LIR_Nem_3 | 2 | 7 | PF02991 | 0.677 |
LIG_LIR_Nem_3 | 67 | 71 | PF02991 | 0.630 |
LIG_MYND_1 | 56 | 60 | PF01753 | 0.733 |
LIG_Pex14_1 | 261 | 265 | PF04695 | 0.662 |
LIG_SH2_NCK_1 | 266 | 270 | PF00017 | 0.763 |
LIG_SH2_STAT5 | 266 | 269 | PF00017 | 0.758 |
LIG_SH2_STAT5 | 4 | 7 | PF00017 | 0.680 |
LIG_SH3_3 | 12 | 18 | PF00018 | 0.741 |
LIG_SH3_3 | 184 | 190 | PF00018 | 0.556 |
LIG_SH3_3 | 368 | 374 | PF00018 | 0.576 |
LIG_SH3_3 | 57 | 63 | PF00018 | 0.647 |
LIG_SUMO_SIM_par_1 | 170 | 175 | PF11976 | 0.800 |
LIG_TRAF2_1 | 10 | 13 | PF00917 | 0.727 |
LIG_TRAF2_1 | 102 | 105 | PF00917 | 0.542 |
LIG_TRAF2_1 | 213 | 216 | PF00917 | 0.548 |
LIG_TRAF2_1 | 228 | 231 | PF00917 | 0.578 |
LIG_TRAF2_1 | 271 | 274 | PF00917 | 0.643 |
LIG_ULM_U2AF65_1 | 69 | 74 | PF00076 | 0.526 |
LIG_WRC_WIRS_1 | 332 | 337 | PF05994 | 0.793 |
LIG_WW_3 | 16 | 20 | PF00397 | 0.523 |
LIG_WW_3 | 231 | 235 | PF00397 | 0.693 |
MOD_CDK_SPK_2 | 161 | 166 | PF00069 | 0.556 |
MOD_CDK_SPxxK_3 | 298 | 305 | PF00069 | 0.816 |
MOD_CK1_1 | 264 | 270 | PF00069 | 0.750 |
MOD_CK1_1 | 27 | 33 | PF00069 | 0.753 |
MOD_CK1_1 | 86 | 92 | PF00069 | 0.557 |
MOD_CK2_1 | 225 | 231 | PF00069 | 0.590 |
MOD_CK2_1 | 287 | 293 | PF00069 | 0.523 |
MOD_CK2_1 | 316 | 322 | PF00069 | 0.541 |
MOD_CK2_1 | 99 | 105 | PF00069 | 0.543 |
MOD_GlcNHglycan | 243 | 246 | PF01048 | 0.731 |
MOD_GlcNHglycan | 285 | 288 | PF01048 | 0.624 |
MOD_GlcNHglycan | 29 | 32 | PF01048 | 0.658 |
MOD_GlcNHglycan | 296 | 299 | PF01048 | 0.663 |
MOD_GlcNHglycan | 318 | 321 | PF01048 | 0.637 |
MOD_GlcNHglycan | 52 | 55 | PF01048 | 0.668 |
MOD_GlcNHglycan | 88 | 91 | PF01048 | 0.579 |
MOD_GSK3_1 | 105 | 112 | PF00069 | 0.768 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.665 |
MOD_GSK3_1 | 236 | 243 | PF00069 | 0.645 |
MOD_GSK3_1 | 260 | 267 | PF00069 | 0.718 |
MOD_GSK3_1 | 283 | 290 | PF00069 | 0.771 |
MOD_GSK3_1 | 294 | 301 | PF00069 | 0.620 |
MOD_GSK3_1 | 312 | 319 | PF00069 | 0.665 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.651 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.630 |
MOD_N-GLC_1 | 143 | 148 | PF02516 | 0.551 |
MOD_N-GLC_1 | 269 | 274 | PF02516 | 0.607 |
MOD_N-GLC_1 | 294 | 299 | PF02516 | 0.749 |
MOD_NEK2_1 | 265 | 270 | PF00069 | 0.639 |
MOD_NEK2_1 | 304 | 309 | PF00069 | 0.822 |
MOD_NEK2_2 | 261 | 266 | PF00069 | 0.716 |
MOD_OFUCOSY | 201 | 208 | PF10250 | 0.555 |
MOD_PIKK_1 | 349 | 355 | PF00454 | 0.839 |
MOD_PKA_1 | 240 | 246 | PF00069 | 0.529 |
MOD_PKA_1 | 80 | 86 | PF00069 | 0.545 |
MOD_PKA_2 | 236 | 242 | PF00069 | 0.810 |
MOD_PKA_2 | 304 | 310 | PF00069 | 0.820 |
MOD_PKA_2 | 363 | 369 | PF00069 | 0.750 |
MOD_PKA_2 | 80 | 86 | PF00069 | 0.670 |
MOD_Plk_2-3 | 331 | 337 | PF00069 | 0.533 |
MOD_Plk_4 | 118 | 124 | PF00069 | 0.773 |
MOD_Plk_4 | 20 | 26 | PF00069 | 0.549 |
MOD_Plk_4 | 261 | 267 | PF00069 | 0.595 |
MOD_Plk_4 | 287 | 293 | PF00069 | 0.783 |
MOD_Plk_4 | 312 | 318 | PF00069 | 0.804 |
MOD_ProDKin_1 | 161 | 167 | PF00069 | 0.554 |
MOD_ProDKin_1 | 201 | 207 | PF00069 | 0.539 |
MOD_ProDKin_1 | 298 | 304 | PF00069 | 0.814 |
MOD_ProDKin_1 | 56 | 62 | PF00069 | 0.776 |
MOD_SUMO_rev_2 | 154 | 160 | PF00179 | 0.639 |
TRG_DiLeu_BaEn_1 | 175 | 180 | PF01217 | 0.533 |
TRG_DiLeu_BaEn_4 | 215 | 221 | PF01217 | 0.560 |
TRG_DiLeu_BaLyEn_6 | 299 | 304 | PF01217 | 0.560 |
TRG_ER_diArg_1 | 157 | 160 | PF00400 | 0.574 |
TRG_ER_diArg_1 | 184 | 187 | PF00400 | 0.676 |
TRG_ER_diArg_1 | 233 | 235 | PF00400 | 0.714 |
TRG_ER_diArg_1 | 304 | 306 | PF00400 | 0.797 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8ICV9 | Leishmania donovani | 61% | 98% |
A4I7H9 | Leishmania infantum | 61% | 98% |
E9B2D6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 63% | 96% |
Q4Q5S0 | Leishmania major | 64% | 100% |