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: A4IA47
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 138 | 142 | PF00656 | 0.722 |
CLV_C14_Caspase3-7 | 236 | 240 | PF00656 | 0.845 |
CLV_C14_Caspase3-7 | 72 | 76 | PF00656 | 0.759 |
CLV_NRD_NRD_1 | 165 | 167 | PF00675 | 0.689 |
CLV_NRD_NRD_1 | 211 | 213 | PF00675 | 0.767 |
CLV_NRD_NRD_1 | 267 | 269 | PF00675 | 0.600 |
CLV_NRD_NRD_1 | 357 | 359 | PF00675 | 0.571 |
CLV_NRD_NRD_1 | 383 | 385 | PF00675 | 0.511 |
CLV_NRD_NRD_1 | 4 | 6 | PF00675 | 0.727 |
CLV_NRD_NRD_1 | 51 | 53 | PF00675 | 0.763 |
CLV_NRD_NRD_1 | 96 | 98 | PF00675 | 0.834 |
CLV_PCSK_KEX2_1 | 167 | 169 | PF00082 | 0.648 |
CLV_PCSK_KEX2_1 | 211 | 213 | PF00082 | 0.767 |
CLV_PCSK_KEX2_1 | 267 | 269 | PF00082 | 0.508 |
CLV_PCSK_KEX2_1 | 357 | 359 | PF00082 | 0.571 |
CLV_PCSK_KEX2_1 | 382 | 384 | PF00082 | 0.584 |
CLV_PCSK_KEX2_1 | 4 | 6 | PF00082 | 0.727 |
CLV_PCSK_KEX2_1 | 51 | 53 | PF00082 | 0.763 |
CLV_PCSK_KEX2_1 | 95 | 97 | PF00082 | 0.837 |
CLV_PCSK_PC1ET2_1 | 167 | 169 | PF00082 | 0.648 |
CLV_PCSK_PC7_1 | 379 | 385 | PF00082 | 0.539 |
CLV_PCSK_PC7_1 | 92 | 98 | PF00082 | 0.832 |
CLV_PCSK_SKI1_1 | 250 | 254 | PF00082 | 0.698 |
DEG_SCF_FBW7_1 | 176 | 181 | PF00400 | 0.782 |
DEG_SPOP_SBC_1 | 87 | 91 | PF00917 | 0.713 |
DOC_CYCLIN_RxL_1 | 357 | 367 | PF00134 | 0.471 |
DOC_MAPK_gen_1 | 357 | 365 | PF00069 | 0.533 |
DOC_MAPK_gen_1 | 416 | 426 | PF00069 | 0.426 |
DOC_MAPK_gen_1 | 78 | 87 | PF00069 | 0.780 |
DOC_MAPK_MEF2A_6 | 299 | 306 | PF00069 | 0.489 |
DOC_PP1_RVXF_1 | 356 | 363 | PF00149 | 0.541 |
DOC_PP2B_LxvP_1 | 196 | 199 | PF13499 | 0.755 |
DOC_USP7_MATH_1 | 178 | 182 | PF00917 | 0.814 |
DOC_USP7_MATH_1 | 245 | 249 | PF00917 | 0.722 |
DOC_USP7_MATH_1 | 71 | 75 | PF00917 | 0.791 |
DOC_WW_Pin1_4 | 174 | 179 | PF00397 | 0.785 |
DOC_WW_Pin1_4 | 181 | 186 | PF00397 | 0.717 |
DOC_WW_Pin1_4 | 254 | 259 | PF00397 | 0.627 |
DOC_WW_Pin1_4 | 8 | 13 | PF00397 | 0.699 |
LIG_14-3-3_CanoR_1 | 111 | 116 | PF00244 | 0.625 |
LIG_14-3-3_CanoR_1 | 250 | 260 | PF00244 | 0.660 |
LIG_14-3-3_CanoR_1 | 352 | 360 | PF00244 | 0.600 |
LIG_14-3-3_CanoR_1 | 382 | 387 | PF00244 | 0.582 |
LIG_14-3-3_CanoR_1 | 51 | 55 | PF00244 | 0.678 |
LIG_Actin_WH2_2 | 290 | 307 | PF00022 | 0.578 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.784 |
LIG_BIR_III_2 | 197 | 201 | PF00653 | 0.803 |
LIG_FHA_1 | 255 | 261 | PF00498 | 0.730 |
LIG_FHA_1 | 32 | 38 | PF00498 | 0.662 |
LIG_FHA_1 | 398 | 404 | PF00498 | 0.538 |
LIG_FHA_1 | 421 | 427 | PF00498 | 0.406 |
LIG_FHA_1 | 430 | 436 | PF00498 | 0.401 |
LIG_FHA_2 | 231 | 237 | PF00498 | 0.745 |
LIG_FHA_2 | 88 | 94 | PF00498 | 0.688 |
LIG_HCF-1_HBM_1 | 377 | 380 | PF13415 | 0.509 |
LIG_LIR_Gen_1 | 57 | 66 | PF02991 | 0.639 |
LIG_MYND_1 | 258 | 262 | PF01753 | 0.580 |
LIG_Pex14_2 | 317 | 321 | PF04695 | 0.461 |
LIG_Pex14_2 | 407 | 411 | PF04695 | 0.432 |
LIG_REV1ctd_RIR_1 | 314 | 324 | PF16727 | 0.480 |
LIG_SH2_CRK | 122 | 126 | PF00017 | 0.618 |
LIG_SH2_CRK | 276 | 280 | PF00017 | 0.486 |
LIG_SH2_NCK_1 | 122 | 126 | PF00017 | 0.618 |
LIG_SH2_STAP1 | 133 | 137 | PF00017 | 0.770 |
LIG_SH2_STAP1 | 28 | 32 | PF00017 | 0.655 |
LIG_SH2_STAP1 | 64 | 68 | PF00017 | 0.678 |
LIG_SH2_STAT3 | 64 | 67 | PF00017 | 0.682 |
LIG_SH2_STAT5 | 133 | 136 | PF00017 | 0.671 |
LIG_SH2_STAT5 | 296 | 299 | PF00017 | 0.474 |
LIG_SH2_STAT5 | 380 | 383 | PF00017 | 0.518 |
LIG_SH2_STAT5 | 402 | 405 | PF00017 | 0.520 |
LIG_SH2_STAT5 | 434 | 437 | PF00017 | 0.533 |
LIG_SH2_STAT5 | 60 | 63 | PF00017 | 0.710 |
LIG_SH2_STAT5 | 64 | 67 | PF00017 | 0.687 |
LIG_SH3_1 | 187 | 193 | PF00018 | 0.688 |
LIG_SH3_1 | 277 | 283 | PF00018 | 0.631 |
LIG_SH3_3 | 102 | 108 | PF00018 | 0.696 |
LIG_SH3_3 | 187 | 193 | PF00018 | 0.778 |
LIG_SH3_3 | 276 | 282 | PF00018 | 0.463 |
LIG_SUMO_SIM_anti_2 | 421 | 429 | PF11976 | 0.568 |
LIG_TRAF2_1 | 148 | 151 | PF00917 | 0.723 |
LIG_WRC_WIRS_1 | 440 | 445 | PF05994 | 0.429 |
MOD_CDC14_SPxK_1 | 184 | 187 | PF00782 | 0.685 |
MOD_CDK_SPxK_1 | 181 | 187 | PF00069 | 0.698 |
MOD_CK1_1 | 100 | 106 | PF00069 | 0.840 |
MOD_CK1_1 | 126 | 132 | PF00069 | 0.756 |
MOD_CK1_1 | 174 | 180 | PF00069 | 0.779 |
MOD_CK1_1 | 181 | 187 | PF00069 | 0.731 |
MOD_CK1_1 | 254 | 260 | PF00069 | 0.617 |
MOD_CK1_1 | 298 | 304 | PF00069 | 0.522 |
MOD_CK1_1 | 353 | 359 | PF00069 | 0.404 |
MOD_CK1_1 | 415 | 421 | PF00069 | 0.519 |
MOD_CK1_1 | 442 | 448 | PF00069 | 0.424 |
MOD_CK1_1 | 47 | 53 | PF00069 | 0.724 |
MOD_CK2_1 | 144 | 150 | PF00069 | 0.721 |
MOD_CK2_1 | 415 | 421 | PF00069 | 0.519 |
MOD_Cter_Amidation | 209 | 212 | PF01082 | 0.768 |
MOD_GlcNHglycan | 102 | 105 | PF01048 | 0.830 |
MOD_GlcNHglycan | 12 | 15 | PF01048 | 0.751 |
MOD_GlcNHglycan | 137 | 140 | PF01048 | 0.800 |
MOD_GlcNHglycan | 180 | 183 | PF01048 | 0.753 |
MOD_GlcNHglycan | 23 | 27 | PF01048 | 0.703 |
MOD_GlcNHglycan | 253 | 256 | PF01048 | 0.697 |
MOD_GlcNHglycan | 352 | 355 | PF01048 | 0.499 |
MOD_GlcNHglycan | 395 | 398 | PF01048 | 0.677 |
MOD_GSK3_1 | 123 | 130 | PF00069 | 0.723 |
MOD_GSK3_1 | 131 | 138 | PF00069 | 0.615 |
MOD_GSK3_1 | 170 | 177 | PF00069 | 0.729 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.739 |
MOD_GSK3_1 | 220 | 227 | PF00069 | 0.820 |
MOD_GSK3_1 | 256 | 263 | PF00069 | 0.581 |
MOD_GSK3_1 | 346 | 353 | PF00069 | 0.531 |
MOD_GSK3_1 | 393 | 400 | PF00069 | 0.554 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.745 |
MOD_N-GLC_1 | 220 | 225 | PF02516 | 0.700 |
MOD_N-GLC_1 | 429 | 434 | PF02516 | 0.452 |
MOD_N-GLC_1 | 47 | 52 | PF02516 | 0.685 |
MOD_NEK2_1 | 325 | 330 | PF00069 | 0.586 |
MOD_NEK2_1 | 398 | 403 | PF00069 | 0.438 |
MOD_NEK2_2 | 245 | 250 | PF00069 | 0.663 |
MOD_PIKK_1 | 429 | 435 | PF00454 | 0.458 |
MOD_PIKK_1 | 442 | 448 | PF00454 | 0.479 |
MOD_PK_1 | 111 | 117 | PF00069 | 0.625 |
MOD_PKA_1 | 382 | 388 | PF00069 | 0.589 |
MOD_PKA_2 | 100 | 106 | PF00069 | 0.840 |
MOD_PKA_2 | 21 | 27 | PF00069 | 0.767 |
MOD_PKA_2 | 298 | 304 | PF00069 | 0.427 |
MOD_PKA_2 | 339 | 345 | PF00069 | 0.458 |
MOD_PKA_2 | 382 | 388 | PF00069 | 0.536 |
MOD_PKA_2 | 415 | 421 | PF00069 | 0.519 |
MOD_PKA_2 | 50 | 56 | PF00069 | 0.799 |
MOD_PKB_1 | 166 | 174 | PF00069 | 0.675 |
MOD_PKB_1 | 95 | 103 | PF00069 | 0.836 |
MOD_Plk_1 | 420 | 426 | PF00069 | 0.472 |
MOD_Plk_1 | 429 | 435 | PF00069 | 0.475 |
MOD_Plk_2-3 | 146 | 152 | PF00069 | 0.727 |
MOD_Plk_4 | 298 | 304 | PF00069 | 0.584 |
MOD_Plk_4 | 339 | 345 | PF00069 | 0.639 |
MOD_Plk_4 | 346 | 352 | PF00069 | 0.442 |
MOD_Plk_4 | 398 | 404 | PF00069 | 0.441 |
MOD_Plk_4 | 439 | 445 | PF00069 | 0.383 |
MOD_ProDKin_1 | 174 | 180 | PF00069 | 0.785 |
MOD_ProDKin_1 | 181 | 187 | PF00069 | 0.721 |
MOD_ProDKin_1 | 254 | 260 | PF00069 | 0.612 |
MOD_ProDKin_1 | 8 | 14 | PF00069 | 0.698 |
MOD_SUMO_rev_2 | 220 | 225 | PF00179 | 0.767 |
MOD_SUMO_rev_2 | 367 | 373 | PF00179 | 0.433 |
TRG_DiLeu_BaEn_1 | 422 | 427 | PF01217 | 0.425 |
TRG_DiLeu_BaLyEn_6 | 248 | 253 | PF01217 | 0.721 |
TRG_ENDOCYTIC_2 | 276 | 279 | PF00928 | 0.440 |
TRG_ENDOCYTIC_2 | 60 | 63 | PF00928 | 0.732 |
TRG_ER_diArg_1 | 211 | 214 | PF00400 | 0.684 |
TRG_ER_diArg_1 | 266 | 268 | PF00400 | 0.546 |
TRG_ER_diArg_1 | 357 | 359 | PF00400 | 0.571 |
TRG_ER_diArg_1 | 381 | 384 | PF00400 | 0.563 |
TRG_ER_diArg_1 | 4 | 7 | PF00400 | 0.707 |
TRG_ER_diArg_1 | 95 | 97 | PF00400 | 0.827 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZ09 | Leptomonas seymouri | 50% | 92% |
A0A3Q8IIN3 | Leishmania donovani | 99% | 100% |
A4HAY8 | Leishmania braziliensis | 68% | 100% |
E9B561 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |