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: A4HC45
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 351 | 355 | PF00656 | 0.756 |
CLV_NRD_NRD_1 | 263 | 265 | PF00675 | 0.725 |
CLV_NRD_NRD_1 | 342 | 344 | PF00675 | 0.709 |
CLV_NRD_NRD_1 | 80 | 82 | PF00675 | 0.674 |
CLV_NRD_NRD_1 | 99 | 101 | PF00675 | 0.479 |
CLV_PCSK_KEX2_1 | 263 | 265 | PF00082 | 0.725 |
CLV_PCSK_KEX2_1 | 342 | 344 | PF00082 | 0.709 |
CLV_PCSK_KEX2_1 | 80 | 82 | PF00082 | 0.674 |
CLV_PCSK_KEX2_1 | 99 | 101 | PF00082 | 0.479 |
CLV_PCSK_SKI1_1 | 104 | 108 | PF00082 | 0.512 |
CLV_PCSK_SKI1_1 | 227 | 231 | PF00082 | 0.655 |
CLV_PCSK_SKI1_1 | 330 | 334 | PF00082 | 0.461 |
CLV_PCSK_SKI1_1 | 342 | 346 | PF00082 | 0.445 |
CLV_PCSK_SKI1_1 | 80 | 84 | PF00082 | 0.667 |
CLV_Separin_Metazoa | 241 | 245 | PF03568 | 0.437 |
DEG_APCC_DBOX_1 | 329 | 337 | PF00400 | 0.453 |
DEG_SPOP_SBC_1 | 23 | 27 | PF00917 | 0.608 |
DEG_SPOP_SBC_1 | 58 | 62 | PF00917 | 0.532 |
DOC_CYCLIN_yCln2_LP_2 | 190 | 196 | PF00134 | 0.478 |
DOC_MAPK_gen_1 | 80 | 88 | PF00069 | 0.677 |
DOC_MAPK_gen_1 | 99 | 107 | PF00069 | 0.462 |
DOC_MAPK_RevD_3 | 66 | 81 | PF00069 | 0.484 |
DOC_PP2B_LxvP_1 | 190 | 193 | PF13499 | 0.476 |
DOC_PP2B_LxvP_1 | 290 | 293 | PF13499 | 0.606 |
DOC_PP2B_LxvP_1 | 56 | 59 | PF13499 | 0.530 |
DOC_USP7_MATH_1 | 108 | 112 | PF00917 | 0.517 |
DOC_USP7_MATH_1 | 176 | 180 | PF00917 | 0.596 |
DOC_USP7_MATH_1 | 23 | 27 | PF00917 | 0.733 |
DOC_USP7_MATH_1 | 234 | 238 | PF00917 | 0.721 |
DOC_USP7_MATH_1 | 276 | 280 | PF00917 | 0.569 |
DOC_USP7_MATH_1 | 296 | 300 | PF00917 | 0.655 |
DOC_USP7_MATH_1 | 338 | 342 | PF00917 | 0.439 |
DOC_USP7_MATH_1 | 4 | 8 | PF00917 | 0.650 |
DOC_USP7_MATH_1 | 50 | 54 | PF00917 | 0.650 |
DOC_USP7_MATH_1 | 57 | 61 | PF00917 | 0.707 |
DOC_WW_Pin1_4 | 11 | 16 | PF00397 | 0.746 |
DOC_WW_Pin1_4 | 133 | 138 | PF00397 | 0.607 |
DOC_WW_Pin1_4 | 188 | 193 | PF00397 | 0.486 |
DOC_WW_Pin1_4 | 249 | 254 | PF00397 | 0.705 |
DOC_WW_Pin1_4 | 269 | 274 | PF00397 | 0.406 |
DOC_WW_Pin1_4 | 288 | 293 | PF00397 | 0.443 |
DOC_WW_Pin1_4 | 313 | 318 | PF00397 | 0.721 |
DOC_WW_Pin1_4 | 39 | 44 | PF00397 | 0.437 |
DOC_WW_Pin1_4 | 422 | 427 | PF00397 | 0.732 |
DOC_WW_Pin1_4 | 88 | 93 | PF00397 | 0.737 |
LIG_14-3-3_CanoR_1 | 342 | 350 | PF00244 | 0.640 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.563 |
LIG_BIR_III_2 | 354 | 358 | PF00653 | 0.686 |
LIG_FHA_1 | 116 | 122 | PF00498 | 0.736 |
LIG_FHA_1 | 147 | 153 | PF00498 | 0.647 |
LIG_FHA_1 | 46 | 52 | PF00498 | 0.687 |
LIG_GBD_Chelix_1 | 254 | 262 | PF00786 | 0.656 |
LIG_LIR_Gen_1 | 30 | 37 | PF02991 | 0.613 |
LIG_LIR_Gen_1 | 386 | 394 | PF02991 | 0.653 |
LIG_LIR_Nem_3 | 136 | 142 | PF02991 | 0.655 |
LIG_LIR_Nem_3 | 30 | 35 | PF02991 | 0.553 |
LIG_LIR_Nem_3 | 386 | 392 | PF02991 | 0.653 |
LIG_PCNA_yPIPBox_3 | 236 | 244 | PF02747 | 0.658 |
LIG_PDZ_Class_2 | 432 | 437 | PF00595 | 0.701 |
LIG_PDZ_Wminus1_1 | 435 | 437 | PF00595 | 0.707 |
LIG_SH2_CRK | 389 | 393 | PF00017 | 0.642 |
LIG_SH2_PTP2 | 141 | 144 | PF00017 | 0.607 |
LIG_SH2_PTP2 | 32 | 35 | PF00017 | 0.620 |
LIG_SH2_SRC | 32 | 35 | PF00017 | 0.620 |
LIG_SH2_STAP1 | 323 | 327 | PF00017 | 0.649 |
LIG_SH2_STAP1 | 45 | 49 | PF00017 | 0.669 |
LIG_SH2_STAT5 | 141 | 144 | PF00017 | 0.607 |
LIG_SH2_STAT5 | 287 | 290 | PF00017 | 0.585 |
LIG_SH2_STAT5 | 32 | 35 | PF00017 | 0.620 |
LIG_SH2_STAT5 | 411 | 414 | PF00017 | 0.687 |
LIG_SH3_3 | 102 | 108 | PF00018 | 0.519 |
LIG_SH3_3 | 141 | 147 | PF00018 | 0.611 |
LIG_SH3_3 | 290 | 296 | PF00018 | 0.543 |
LIG_SH3_3 | 314 | 320 | PF00018 | 0.642 |
LIG_SUMO_SIM_anti_2 | 237 | 244 | PF11976 | 0.446 |
LIG_SUMO_SIM_par_1 | 85 | 91 | PF11976 | 0.706 |
LIG_TRAF2_1 | 299 | 302 | PF00917 | 0.566 |
LIG_TRFH_1 | 288 | 292 | PF08558 | 0.454 |
LIG_TYR_ITIM | 387 | 392 | PF00017 | 0.443 |
LIG_Vh1_VBS_1 | 107 | 125 | PF01044 | 0.497 |
LIG_WW_1 | 137 | 140 | PF00397 | 0.663 |
LIG_WW_3 | 398 | 402 | PF00397 | 0.489 |
MOD_CDK_SPK_2 | 11 | 16 | PF00069 | 0.524 |
MOD_CK1_1 | 111 | 117 | PF00069 | 0.547 |
MOD_CK1_1 | 25 | 31 | PF00069 | 0.564 |
MOD_CK1_1 | 272 | 278 | PF00069 | 0.724 |
MOD_CK1_1 | 291 | 297 | PF00069 | 0.476 |
MOD_CK1_1 | 313 | 319 | PF00069 | 0.738 |
MOD_CK1_1 | 62 | 68 | PF00069 | 0.671 |
MOD_CK2_1 | 235 | 241 | PF00069 | 0.469 |
MOD_CK2_1 | 296 | 302 | PF00069 | 0.559 |
MOD_GlcNHglycan | 130 | 133 | PF01048 | 0.424 |
MOD_GlcNHglycan | 178 | 181 | PF01048 | 0.532 |
MOD_GlcNHglycan | 232 | 235 | PF01048 | 0.655 |
MOD_GlcNHglycan | 27 | 30 | PF01048 | 0.669 |
MOD_GlcNHglycan | 298 | 301 | PF01048 | 0.682 |
MOD_GlcNHglycan | 310 | 313 | PF01048 | 0.801 |
MOD_GlcNHglycan | 325 | 328 | PF01048 | 0.486 |
MOD_GlcNHglycan | 366 | 369 | PF01048 | 0.698 |
MOD_GlcNHglycan | 416 | 419 | PF01048 | 0.507 |
MOD_GlcNHglycan | 61 | 64 | PF01048 | 0.684 |
MOD_GSK3_1 | 111 | 118 | PF00069 | 0.662 |
MOD_GSK3_1 | 230 | 237 | PF00069 | 0.645 |
MOD_GSK3_1 | 245 | 252 | PF00069 | 0.606 |
MOD_GSK3_1 | 272 | 279 | PF00069 | 0.742 |
MOD_GSK3_1 | 338 | 345 | PF00069 | 0.451 |
MOD_GSK3_1 | 58 | 65 | PF00069 | 0.679 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.724 |
MOD_NEK2_1 | 121 | 126 | PF00069 | 0.712 |
MOD_NEK2_1 | 161 | 166 | PF00069 | 0.633 |
MOD_NEK2_1 | 230 | 235 | PF00069 | 0.650 |
MOD_NEK2_1 | 280 | 285 | PF00069 | 0.617 |
MOD_NEK2_1 | 363 | 368 | PF00069 | 0.570 |
MOD_NEK2_1 | 431 | 436 | PF00069 | 0.607 |
MOD_NEK2_2 | 276 | 281 | PF00069 | 0.477 |
MOD_PIKK_1 | 198 | 204 | PF00454 | 0.680 |
MOD_PKA_1 | 342 | 348 | PF00069 | 0.488 |
MOD_PKA_2 | 342 | 348 | PF00069 | 0.488 |
MOD_Plk_1 | 115 | 121 | PF00069 | 0.508 |
MOD_Plk_4 | 116 | 122 | PF00069 | 0.509 |
MOD_Plk_4 | 161 | 167 | PF00069 | 0.636 |
MOD_Plk_4 | 235 | 241 | PF00069 | 0.502 |
MOD_Plk_4 | 257 | 263 | PF00069 | 0.560 |
MOD_Plk_4 | 383 | 389 | PF00069 | 0.476 |
MOD_ProDKin_1 | 11 | 17 | PF00069 | 0.746 |
MOD_ProDKin_1 | 133 | 139 | PF00069 | 0.606 |
MOD_ProDKin_1 | 188 | 194 | PF00069 | 0.489 |
MOD_ProDKin_1 | 249 | 255 | PF00069 | 0.696 |
MOD_ProDKin_1 | 269 | 275 | PF00069 | 0.404 |
MOD_ProDKin_1 | 288 | 294 | PF00069 | 0.453 |
MOD_ProDKin_1 | 313 | 319 | PF00069 | 0.720 |
MOD_ProDKin_1 | 39 | 45 | PF00069 | 0.433 |
MOD_ProDKin_1 | 422 | 428 | PF00069 | 0.733 |
MOD_ProDKin_1 | 88 | 94 | PF00069 | 0.741 |
TRG_DiLeu_BaEn_1 | 116 | 121 | PF01217 | 0.509 |
TRG_DiLeu_BaEn_1 | 331 | 336 | PF01217 | 0.663 |
TRG_DiLeu_BaEn_4 | 301 | 307 | PF01217 | 0.563 |
TRG_DiLeu_LyEn_5 | 331 | 336 | PF01217 | 0.663 |
TRG_ENDOCYTIC_2 | 139 | 142 | PF00928 | 0.625 |
TRG_ENDOCYTIC_2 | 287 | 290 | PF00928 | 0.585 |
TRG_ENDOCYTIC_2 | 32 | 35 | PF00928 | 0.620 |
TRG_ENDOCYTIC_2 | 389 | 392 | PF00928 | 0.643 |
TRG_ER_diArg_1 | 262 | 264 | PF00400 | 0.583 |
TRG_ER_diArg_1 | 79 | 81 | PF00400 | 0.667 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IKQ2 | Leptomonas seymouri | 34% | 100% |
A0A3S5H698 | Leishmania donovani | 72% | 100% |
E9ACQ6 | Leishmania major | 72% | 97% |
E9AG91 | Leishmania infantum | 72% | 100% |
E9AMJ5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 71% | 80% |