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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: E9B4L0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 276 | 280 | PF00656 | 0.462 |
CLV_C14_Caspase3-7 | 62 | 66 | PF00656 | 0.673 |
CLV_MEL_PAP_1 | 193 | 199 | PF00089 | 0.579 |
CLV_NRD_NRD_1 | 167 | 169 | PF00675 | 0.503 |
CLV_NRD_NRD_1 | 405 | 407 | PF00675 | 0.565 |
CLV_NRD_NRD_1 | 97 | 99 | PF00675 | 0.673 |
CLV_PCSK_KEX2_1 | 167 | 169 | PF00082 | 0.503 |
CLV_PCSK_KEX2_1 | 405 | 407 | PF00082 | 0.565 |
CLV_PCSK_KEX2_1 | 97 | 99 | PF00082 | 0.670 |
CLV_PCSK_SKI1_1 | 179 | 183 | PF00082 | 0.649 |
CLV_PCSK_SKI1_1 | 223 | 227 | PF00082 | 0.649 |
CLV_Separin_Metazoa | 365 | 369 | PF03568 | 0.539 |
DEG_APCC_DBOX_1 | 195 | 203 | PF00400 | 0.619 |
DEG_SCF_FBW7_2 | 107 | 113 | PF00400 | 0.508 |
DEG_SPOP_SBC_1 | 382 | 386 | PF00917 | 0.509 |
DOC_CKS1_1 | 107 | 112 | PF01111 | 0.508 |
DOC_CKS1_1 | 67 | 72 | PF01111 | 0.734 |
DOC_CKS1_1 | 84 | 89 | PF01111 | 0.741 |
DOC_MAPK_gen_1 | 245 | 253 | PF00069 | 0.585 |
DOC_MAPK_gen_1 | 388 | 395 | PF00069 | 0.691 |
DOC_MAPK_MEF2A_6 | 191 | 199 | PF00069 | 0.588 |
DOC_MAPK_MEF2A_6 | 247 | 255 | PF00069 | 0.564 |
DOC_MAPK_RevD_3 | 154 | 168 | PF00069 | 0.383 |
DOC_PP1_RVXF_1 | 366 | 372 | PF00149 | 0.539 |
DOC_PP1_RVXF_1 | 56 | 62 | PF00149 | 0.578 |
DOC_PP2B_LxvP_1 | 255 | 258 | PF13499 | 0.608 |
DOC_USP7_MATH_1 | 144 | 148 | PF00917 | 0.709 |
DOC_USP7_MATH_1 | 173 | 177 | PF00917 | 0.667 |
DOC_USP7_MATH_1 | 195 | 199 | PF00917 | 0.496 |
DOC_USP7_MATH_1 | 2 | 6 | PF00917 | 0.668 |
DOC_USP7_MATH_1 | 209 | 213 | PF00917 | 0.637 |
DOC_USP7_MATH_1 | 318 | 322 | PF00917 | 0.628 |
DOC_USP7_MATH_1 | 348 | 352 | PF00917 | 0.581 |
DOC_WW_Pin1_4 | 106 | 111 | PF00397 | 0.704 |
DOC_WW_Pin1_4 | 171 | 176 | PF00397 | 0.606 |
DOC_WW_Pin1_4 | 66 | 71 | PF00397 | 0.696 |
DOC_WW_Pin1_4 | 83 | 88 | PF00397 | 0.810 |
DOC_WW_Pin1_4 | 9 | 14 | PF00397 | 0.598 |
LIG_14-3-3_CanoR_1 | 130 | 135 | PF00244 | 0.515 |
LIG_14-3-3_CanoR_1 | 196 | 200 | PF00244 | 0.606 |
LIG_14-3-3_CanoR_1 | 320 | 326 | PF00244 | 0.668 |
LIG_14-3-3_CanoR_1 | 394 | 401 | PF00244 | 0.672 |
LIG_Actin_WH2_2 | 186 | 202 | PF00022 | 0.595 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.617 |
LIG_BRCT_BRCA1_1 | 29 | 33 | PF00533 | 0.545 |
LIG_Clathr_ClatBox_1 | 156 | 160 | PF01394 | 0.598 |
LIG_FHA_1 | 143 | 149 | PF00498 | 0.698 |
LIG_FHA_1 | 226 | 232 | PF00498 | 0.532 |
LIG_FHA_1 | 269 | 275 | PF00498 | 0.489 |
LIG_FHA_1 | 37 | 43 | PF00498 | 0.642 |
LIG_FHA_1 | 377 | 383 | PF00498 | 0.511 |
LIG_FHA_2 | 373 | 379 | PF00498 | 0.689 |
LIG_FHA_2 | 382 | 388 | PF00498 | 0.595 |
LIG_FHA_2 | 55 | 61 | PF00498 | 0.647 |
LIG_HP1_1 | 195 | 199 | PF01393 | 0.593 |
LIG_LIR_Apic_2 | 12 | 17 | PF02991 | 0.593 |
LIG_LIR_Gen_1 | 180 | 189 | PF02991 | 0.599 |
LIG_LIR_Nem_3 | 180 | 185 | PF02991 | 0.616 |
LIG_SH2_PTP2 | 14 | 17 | PF00017 | 0.717 |
LIG_SH2_SRC | 14 | 17 | PF00017 | 0.645 |
LIG_SH2_STAT3 | 230 | 233 | PF00017 | 0.606 |
LIG_SH2_STAT5 | 14 | 17 | PF00017 | 0.733 |
LIG_SH2_STAT5 | 230 | 233 | PF00017 | 0.606 |
LIG_SH2_STAT5 | 38 | 41 | PF00017 | 0.544 |
LIG_SH3_1 | 10 | 16 | PF00018 | 0.631 |
LIG_SH3_1 | 167 | 173 | PF00018 | 0.699 |
LIG_SH3_3 | 10 | 16 | PF00018 | 0.706 |
LIG_SH3_3 | 104 | 110 | PF00018 | 0.754 |
LIG_SH3_3 | 167 | 173 | PF00018 | 0.774 |
LIG_SH3_3 | 229 | 235 | PF00018 | 0.492 |
LIG_SH3_3 | 81 | 87 | PF00018 | 0.776 |
LIG_SH3_3 | 90 | 96 | PF00018 | 0.633 |
LIG_SUMO_SIM_anti_2 | 248 | 254 | PF11976 | 0.560 |
LIG_SUMO_SIM_par_1 | 155 | 160 | PF11976 | 0.593 |
LIG_SUMO_SIM_par_1 | 248 | 254 | PF11976 | 0.500 |
LIG_SUMO_SIM_par_1 | 351 | 358 | PF11976 | 0.542 |
LIG_TRAF2_1 | 111 | 114 | PF00917 | 0.708 |
LIG_WRC_WIRS_1 | 4 | 9 | PF05994 | 0.655 |
MOD_CDK_SPxK_1 | 66 | 72 | PF00069 | 0.683 |
MOD_CK1_1 | 116 | 122 | PF00069 | 0.625 |
MOD_CK1_1 | 162 | 168 | PF00069 | 0.613 |
MOD_CK1_1 | 268 | 274 | PF00069 | 0.746 |
MOD_CK1_1 | 321 | 327 | PF00069 | 0.645 |
MOD_CK1_1 | 355 | 361 | PF00069 | 0.664 |
MOD_CK1_1 | 389 | 395 | PF00069 | 0.763 |
MOD_CK1_1 | 66 | 72 | PF00069 | 0.533 |
MOD_CK2_1 | 2 | 8 | PF00069 | 0.747 |
MOD_CK2_1 | 372 | 378 | PF00069 | 0.671 |
MOD_CK2_1 | 381 | 387 | PF00069 | 0.597 |
MOD_CK2_1 | 54 | 60 | PF00069 | 0.780 |
MOD_Cter_Amidation | 165 | 168 | PF01082 | 0.475 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.591 |
MOD_GlcNHglycan | 275 | 278 | PF01048 | 0.518 |
MOD_GlcNHglycan | 323 | 326 | PF01048 | 0.747 |
MOD_GlcNHglycan | 47 | 53 | PF01048 | 0.652 |
MOD_GlcNHglycan | 87 | 90 | PF01048 | 0.825 |
MOD_GSK3_1 | 112 | 119 | PF00069 | 0.702 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.674 |
MOD_GSK3_1 | 241 | 248 | PF00069 | 0.517 |
MOD_GSK3_1 | 261 | 268 | PF00069 | 0.539 |
MOD_GSK3_1 | 269 | 276 | PF00069 | 0.655 |
MOD_GSK3_1 | 328 | 335 | PF00069 | 0.658 |
MOD_GSK3_1 | 342 | 349 | PF00069 | 0.429 |
MOD_GSK3_1 | 372 | 379 | PF00069 | 0.670 |
MOD_GSK3_1 | 382 | 389 | PF00069 | 0.699 |
MOD_NEK2_1 | 159 | 164 | PF00069 | 0.584 |
MOD_NEK2_1 | 181 | 186 | PF00069 | 0.616 |
MOD_NEK2_1 | 226 | 231 | PF00069 | 0.511 |
MOD_NEK2_1 | 262 | 267 | PF00069 | 0.510 |
MOD_NEK2_1 | 354 | 359 | PF00069 | 0.564 |
MOD_NEK2_1 | 393 | 398 | PF00069 | 0.671 |
MOD_NEK2_2 | 195 | 200 | PF00069 | 0.608 |
MOD_NEK2_2 | 63 | 68 | PF00069 | 0.543 |
MOD_OFUCOSY | 35 | 40 | PF10250 | 0.622 |
MOD_PIKK_1 | 303 | 309 | PF00454 | 0.443 |
MOD_PIKK_1 | 348 | 354 | PF00454 | 0.541 |
MOD_PIKK_1 | 393 | 399 | PF00454 | 0.624 |
MOD_PK_1 | 130 | 136 | PF00069 | 0.328 |
MOD_PK_1 | 245 | 251 | PF00069 | 0.497 |
MOD_PKA_2 | 195 | 201 | PF00069 | 0.615 |
MOD_PKA_2 | 319 | 325 | PF00069 | 0.663 |
MOD_PKA_2 | 389 | 395 | PF00069 | 0.689 |
MOD_PKA_2 | 63 | 69 | PF00069 | 0.737 |
MOD_Plk_4 | 130 | 136 | PF00069 | 0.328 |
MOD_Plk_4 | 159 | 165 | PF00069 | 0.663 |
MOD_Plk_4 | 226 | 232 | PF00069 | 0.532 |
MOD_ProDKin_1 | 106 | 112 | PF00069 | 0.702 |
MOD_ProDKin_1 | 171 | 177 | PF00069 | 0.596 |
MOD_ProDKin_1 | 66 | 72 | PF00069 | 0.698 |
MOD_ProDKin_1 | 83 | 89 | PF00069 | 0.812 |
MOD_ProDKin_1 | 9 | 15 | PF00069 | 0.605 |
MOD_SUMO_for_1 | 280 | 283 | PF00179 | 0.611 |
MOD_SUMO_rev_2 | 273 | 282 | PF00179 | 0.741 |
TRG_DiLeu_BaEn_1 | 365 | 370 | PF01217 | 0.536 |
TRG_DiLeu_BaLyEn_6 | 197 | 202 | PF01217 | 0.613 |
TRG_DiLeu_BaLyEn_6 | 211 | 216 | PF01217 | 0.516 |
TRG_DiLeu_LyEn_5 | 365 | 370 | PF01217 | 0.536 |
TRG_ER_diArg_1 | 405 | 407 | PF00400 | 0.565 |
TRG_ER_diArg_1 | 96 | 98 | PF00400 | 0.712 |
TRG_Pf-PMV_PEXEL_1 | 179 | 183 | PF00026 | 0.574 |
TRG_Pf-PMV_PEXEL_1 | 214 | 218 | PF00026 | 0.494 |
TRG_Pf-PMV_PEXEL_1 | 405 | 409 | PF00026 | 0.555 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDW8 | Leptomonas seymouri | 37% | 72% |
A0A3S7X7D6 | Leishmania donovani | 87% | 100% |
A4HAF6 | Leishmania braziliensis | 71% | 98% |
A4I9L2 | Leishmania infantum | 87% | 100% |
Q4Q3G6 | Leishmania major | 88% | 100% |