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: 7 |
NetGPI | no | yes: 0, no: 7 |
Related structures:
AlphaFold database: A0A3Q8IBZ5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 170 | 172 | PF00675 | 0.552 |
CLV_NRD_NRD_1 | 311 | 313 | PF00675 | 0.517 |
CLV_NRD_NRD_1 | 321 | 323 | PF00675 | 0.530 |
CLV_NRD_NRD_1 | 78 | 80 | PF00675 | 0.666 |
CLV_PCSK_FUR_1 | 45 | 49 | PF00082 | 0.714 |
CLV_PCSK_KEX2_1 | 311 | 313 | PF00082 | 0.511 |
CLV_PCSK_KEX2_1 | 321 | 323 | PF00082 | 0.530 |
CLV_PCSK_KEX2_1 | 47 | 49 | PF00082 | 0.707 |
CLV_PCSK_PC1ET2_1 | 47 | 49 | PF00082 | 0.707 |
CLV_PCSK_SKI1_1 | 123 | 127 | PF00082 | 0.682 |
CLV_PCSK_SKI1_1 | 177 | 181 | PF00082 | 0.499 |
CLV_PCSK_SKI1_1 | 321 | 325 | PF00082 | 0.508 |
CLV_PCSK_SKI1_1 | 80 | 84 | PF00082 | 0.671 |
CLV_Separin_Metazoa | 42 | 46 | PF03568 | 0.597 |
DEG_SCF_FBW7_2 | 222 | 228 | PF00400 | 0.644 |
DOC_CDC14_PxL_1 | 103 | 111 | PF14671 | 0.659 |
DOC_CKS1_1 | 222 | 227 | PF01111 | 0.634 |
DOC_CYCLIN_RxL_1 | 318 | 327 | PF00134 | 0.487 |
DOC_MAPK_gen_1 | 318 | 328 | PF00069 | 0.548 |
DOC_MAPK_gen_1 | 337 | 346 | PF00069 | 0.569 |
DOC_PP1_RVXF_1 | 170 | 177 | PF00149 | 0.489 |
DOC_PP1_RVXF_1 | 284 | 290 | PF00149 | 0.694 |
DOC_USP7_MATH_1 | 264 | 268 | PF00917 | 0.774 |
DOC_USP7_MATH_1 | 305 | 309 | PF00917 | 0.745 |
DOC_USP7_MATH_1 | 92 | 96 | PF00917 | 0.661 |
DOC_USP7_UBL2_3 | 80 | 84 | PF12436 | 0.671 |
DOC_WW_Pin1_4 | 221 | 226 | PF00397 | 0.564 |
DOC_WW_Pin1_4 | 83 | 88 | PF00397 | 0.748 |
LIG_14-3-3_CanoR_1 | 10 | 18 | PF00244 | 0.716 |
LIG_14-3-3_CanoR_1 | 123 | 130 | PF00244 | 0.599 |
LIG_14-3-3_CanoR_1 | 171 | 177 | PF00244 | 0.510 |
LIG_14-3-3_CanoR_1 | 212 | 222 | PF00244 | 0.540 |
LIG_14-3-3_CanoR_1 | 45 | 55 | PF00244 | 0.700 |
LIG_BRCT_BRCA1_1 | 222 | 226 | PF00533 | 0.561 |
LIG_Clathr_ClatBox_1 | 323 | 327 | PF01394 | 0.487 |
LIG_Clathr_ClatBox_1 | 332 | 336 | PF01394 | 0.505 |
LIG_FHA_1 | 25 | 31 | PF00498 | 0.685 |
LIG_FHA_1 | 35 | 41 | PF00498 | 0.710 |
LIG_FHA_2 | 124 | 130 | PF00498 | 0.790 |
LIG_LIR_Apic_2 | 240 | 246 | PF02991 | 0.609 |
LIG_LIR_Nem_3 | 200 | 205 | PF02991 | 0.518 |
LIG_SH2_CRK | 183 | 187 | PF00017 | 0.510 |
LIG_SH2_STAT5 | 243 | 246 | PF00017 | 0.656 |
LIG_SH2_STAT5 | 315 | 318 | PF00017 | 0.463 |
LIG_SH3_3 | 219 | 225 | PF00018 | 0.565 |
LIG_SH3_3 | 242 | 248 | PF00018 | 0.639 |
LIG_SH3_3 | 356 | 362 | PF00018 | 0.542 |
LIG_SUMO_SIM_par_1 | 26 | 33 | PF11976 | 0.571 |
LIG_WRC_WIRS_1 | 164 | 169 | PF05994 | 0.621 |
MOD_CK1_1 | 124 | 130 | PF00069 | 0.714 |
MOD_CK1_1 | 146 | 152 | PF00069 | 0.742 |
MOD_CK1_1 | 21 | 27 | PF00069 | 0.607 |
MOD_CK1_1 | 216 | 222 | PF00069 | 0.634 |
MOD_CK1_1 | 29 | 35 | PF00069 | 0.628 |
MOD_CK1_1 | 304 | 310 | PF00069 | 0.682 |
MOD_CK1_1 | 49 | 55 | PF00069 | 0.464 |
MOD_CK2_1 | 123 | 129 | PF00069 | 0.724 |
MOD_Cter_Amidation | 319 | 322 | PF01082 | 0.611 |
MOD_Cter_Amidation | 45 | 48 | PF01082 | 0.719 |
MOD_GlcNHglycan | 109 | 112 | PF01048 | 0.602 |
MOD_GlcNHglycan | 126 | 129 | PF01048 | 0.720 |
MOD_GlcNHglycan | 130 | 133 | PF01048 | 0.723 |
MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.658 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.733 |
MOD_GlcNHglycan | 147 | 151 | PF01048 | 0.703 |
MOD_GlcNHglycan | 153 | 156 | PF01048 | 0.567 |
MOD_GlcNHglycan | 197 | 200 | PF01048 | 0.567 |
MOD_GlcNHglycan | 266 | 269 | PF01048 | 0.758 |
MOD_GlcNHglycan | 282 | 285 | PF01048 | 0.663 |
MOD_GlcNHglycan | 290 | 293 | PF01048 | 0.705 |
MOD_GlcNHglycan | 303 | 306 | PF01048 | 0.583 |
MOD_GlcNHglycan | 48 | 51 | PF01048 | 0.701 |
MOD_GlcNHglycan | 99 | 102 | PF01048 | 0.697 |
MOD_GSK3_1 | 124 | 131 | PF00069 | 0.696 |
MOD_GSK3_1 | 149 | 156 | PF00069 | 0.762 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.632 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.556 |
MOD_GSK3_1 | 26 | 33 | PF00069 | 0.703 |
MOD_GSK3_1 | 288 | 295 | PF00069 | 0.704 |
MOD_GSK3_1 | 301 | 308 | PF00069 | 0.709 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.709 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.694 |
MOD_LATS_1 | 121 | 127 | PF00433 | 0.585 |
MOD_N-GLC_1 | 162 | 167 | PF02516 | 0.704 |
MOD_N-GLC_1 | 172 | 177 | PF02516 | 0.479 |
MOD_N-GLC_1 | 92 | 97 | PF02516 | 0.675 |
MOD_NEK2_1 | 153 | 158 | PF00069 | 0.673 |
MOD_NEK2_1 | 18 | 23 | PF00069 | 0.661 |
MOD_NEK2_1 | 197 | 202 | PF00069 | 0.518 |
MOD_NEK2_1 | 215 | 220 | PF00069 | 0.497 |
MOD_NEK2_1 | 88 | 93 | PF00069 | 0.772 |
MOD_NEK2_1 | 96 | 101 | PF00069 | 0.633 |
MOD_PIKK_1 | 292 | 298 | PF00454 | 0.767 |
MOD_PKA_2 | 78 | 84 | PF00069 | 0.773 |
MOD_PKA_2 | 9 | 15 | PF00069 | 0.753 |
MOD_Plk_1 | 162 | 168 | PF00069 | 0.698 |
MOD_Plk_1 | 172 | 178 | PF00069 | 0.471 |
MOD_Plk_1 | 62 | 68 | PF00069 | 0.577 |
MOD_Plk_1 | 92 | 98 | PF00069 | 0.640 |
MOD_Plk_4 | 163 | 169 | PF00069 | 0.684 |
MOD_Plk_4 | 273 | 279 | PF00069 | 0.790 |
MOD_Plk_4 | 51 | 57 | PF00069 | 0.732 |
MOD_Plk_4 | 92 | 98 | PF00069 | 0.559 |
MOD_ProDKin_1 | 221 | 227 | PF00069 | 0.564 |
MOD_ProDKin_1 | 83 | 89 | PF00069 | 0.745 |
TRG_DiLeu_BaLyEn_6 | 319 | 324 | PF01217 | 0.538 |
TRG_ENDOCYTIC_2 | 183 | 186 | PF00928 | 0.457 |
TRG_ER_diArg_1 | 168 | 171 | PF00400 | 0.637 |
TRG_ER_diArg_1 | 321 | 323 | PF00400 | 0.530 |
TRG_Pf-PMV_PEXEL_1 | 322 | 327 | PF00026 | 0.540 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDM6 | Leptomonas seymouri | 41% | 98% |
A0A3R7KW68 | Trypanosoma rangeli | 39% | 100% |
A4H5V6 | Leishmania braziliensis | 63% | 100% |
A4HU50 | Leishmania infantum | 100% | 100% |
E9AMX9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
Q4QHP7 | Leishmania major | 94% | 100% |