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: A4HHK6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 197 | 201 | PF00656 | 0.564 |
CLV_NRD_NRD_1 | 13 | 15 | PF00675 | 0.553 |
CLV_NRD_NRD_1 | 195 | 197 | PF00675 | 0.728 |
CLV_NRD_NRD_1 | 209 | 211 | PF00675 | 0.648 |
CLV_NRD_NRD_1 | 268 | 270 | PF00675 | 0.814 |
CLV_NRD_NRD_1 | 271 | 273 | PF00675 | 0.785 |
CLV_PCSK_FUR_1 | 269 | 273 | PF00082 | 0.678 |
CLV_PCSK_KEX2_1 | 15 | 17 | PF00082 | 0.557 |
CLV_PCSK_KEX2_1 | 195 | 197 | PF00082 | 0.732 |
CLV_PCSK_KEX2_1 | 209 | 211 | PF00082 | 0.662 |
CLV_PCSK_KEX2_1 | 268 | 270 | PF00082 | 0.804 |
CLV_PCSK_KEX2_1 | 271 | 273 | PF00082 | 0.832 |
CLV_PCSK_PC1ET2_1 | 15 | 17 | PF00082 | 0.557 |
CLV_PCSK_SKI1_1 | 224 | 228 | PF00082 | 0.602 |
CLV_PCSK_SKI1_1 | 248 | 252 | PF00082 | 0.570 |
CLV_PCSK_SKI1_1 | 405 | 409 | PF00082 | 0.650 |
DEG_APCC_DBOX_1 | 209 | 217 | PF00400 | 0.459 |
DEG_SCF_TRCP1_1 | 261 | 266 | PF00400 | 0.596 |
DEG_SPOP_SBC_1 | 100 | 104 | PF00917 | 0.544 |
DOC_CDC14_PxL_1 | 1 | 9 | PF14671 | 0.625 |
DOC_CKS1_1 | 106 | 111 | PF01111 | 0.558 |
DOC_MAPK_DCC_7 | 209 | 218 | PF00069 | 0.454 |
DOC_MAPK_DCC_7 | 37 | 46 | PF00069 | 0.747 |
DOC_MAPK_HePTP_8 | 206 | 218 | PF00069 | 0.469 |
DOC_MAPK_MEF2A_6 | 209 | 218 | PF00069 | 0.523 |
DOC_MAPK_MEF2A_6 | 224 | 231 | PF00069 | 0.529 |
DOC_MAPK_MEF2A_6 | 37 | 46 | PF00069 | 0.747 |
DOC_MAPK_NFAT4_5 | 224 | 232 | PF00069 | 0.535 |
DOC_USP7_MATH_1 | 303 | 307 | PF00917 | 0.815 |
DOC_USP7_MATH_1 | 321 | 325 | PF00917 | 0.755 |
DOC_USP7_MATH_1 | 35 | 39 | PF00917 | 0.641 |
DOC_USP7_MATH_1 | 352 | 356 | PF00917 | 0.732 |
DOC_USP7_MATH_1 | 375 | 379 | PF00917 | 0.687 |
DOC_USP7_MATH_1 | 6 | 10 | PF00917 | 0.533 |
DOC_USP7_MATH_1 | 99 | 103 | PF00917 | 0.669 |
DOC_WW_Pin1_4 | 105 | 110 | PF00397 | 0.641 |
DOC_WW_Pin1_4 | 185 | 190 | PF00397 | 0.780 |
DOC_WW_Pin1_4 | 198 | 203 | PF00397 | 0.538 |
DOC_WW_Pin1_4 | 20 | 25 | PF00397 | 0.532 |
DOC_WW_Pin1_4 | 301 | 306 | PF00397 | 0.823 |
DOC_WW_Pin1_4 | 348 | 353 | PF00397 | 0.642 |
DOC_WW_Pin1_4 | 395 | 400 | PF00397 | 0.669 |
DOC_WW_Pin1_4 | 414 | 419 | PF00397 | 0.658 |
DOC_WW_Pin1_4 | 72 | 77 | PF00397 | 0.565 |
LIG_14-3-3_CanoR_1 | 195 | 199 | PF00244 | 0.703 |
LIG_14-3-3_CanoR_1 | 209 | 213 | PF00244 | 0.698 |
LIG_14-3-3_CanoR_1 | 248 | 253 | PF00244 | 0.675 |
LIG_14-3-3_CanoR_1 | 269 | 277 | PF00244 | 0.747 |
LIG_14-3-3_CanoR_1 | 288 | 298 | PF00244 | 0.743 |
LIG_14-3-3_CanoR_1 | 346 | 352 | PF00244 | 0.591 |
LIG_14-3-3_CanoR_1 | 368 | 373 | PF00244 | 0.644 |
LIG_14-3-3_CanoR_1 | 37 | 41 | PF00244 | 0.706 |
LIG_14-3-3_CanoR_1 | 381 | 391 | PF00244 | 0.509 |
LIG_14-3-3_CanoR_1 | 405 | 410 | PF00244 | 0.651 |
LIG_14-3-3_CanoR_1 | 56 | 62 | PF00244 | 0.548 |
LIG_14-3-3_CanoR_1 | 79 | 83 | PF00244 | 0.609 |
LIG_14-3-3_CanoR_1 | 95 | 99 | PF00244 | 0.718 |
LIG_AP2alpha_2 | 390 | 392 | PF02296 | 0.529 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.627 |
LIG_BIR_III_4 | 341 | 345 | PF00653 | 0.572 |
LIG_FHA_1 | 21 | 27 | PF00498 | 0.682 |
LIG_FHA_1 | 289 | 295 | PF00498 | 0.771 |
LIG_FHA_2 | 106 | 112 | PF00498 | 0.724 |
LIG_IRF3_LxIS_1 | 90 | 97 | PF10401 | 0.515 |
LIG_LIR_Gen_1 | 128 | 138 | PF02991 | 0.430 |
LIG_LIR_Nem_3 | 128 | 134 | PF02991 | 0.444 |
LIG_LIR_Nem_3 | 388 | 392 | PF02991 | 0.573 |
LIG_MYND_1 | 332 | 336 | PF01753 | 0.543 |
LIG_NRBOX | 89 | 95 | PF00104 | 0.662 |
LIG_PDZ_Class_1 | 414 | 419 | PF00595 | 0.508 |
LIG_PTB_Apo_2 | 230 | 237 | PF02174 | 0.546 |
LIG_SH2_CRK | 404 | 408 | PF00017 | 0.507 |
LIG_SH2_STAT5 | 212 | 215 | PF00017 | 0.452 |
LIG_SH3_3 | 103 | 109 | PF00018 | 0.584 |
LIG_SH3_3 | 299 | 305 | PF00018 | 0.813 |
LIG_SH3_3 | 388 | 394 | PF00018 | 0.670 |
LIG_SH3_3 | 62 | 68 | PF00018 | 0.645 |
LIG_SH3_3 | 80 | 86 | PF00018 | 0.617 |
LIG_SUMO_SIM_anti_2 | 125 | 131 | PF11976 | 0.445 |
LIG_SUMO_SIM_anti_2 | 151 | 157 | PF11976 | 0.509 |
LIG_TRAF2_1 | 108 | 111 | PF00917 | 0.773 |
MOD_CDK_SPK_2 | 348 | 353 | PF00069 | 0.598 |
MOD_CDK_SPxxK_3 | 20 | 27 | PF00069 | 0.572 |
MOD_CDK_SPxxK_3 | 72 | 79 | PF00069 | 0.568 |
MOD_CK1_1 | 140 | 146 | PF00069 | 0.490 |
MOD_CK1_1 | 208 | 214 | PF00069 | 0.595 |
MOD_CK1_1 | 240 | 246 | PF00069 | 0.656 |
MOD_CK1_1 | 30 | 36 | PF00069 | 0.635 |
MOD_CK1_1 | 322 | 328 | PF00069 | 0.730 |
MOD_CK1_1 | 348 | 354 | PF00069 | 0.727 |
MOD_CK1_1 | 382 | 388 | PF00069 | 0.610 |
MOD_CK1_1 | 45 | 51 | PF00069 | 0.744 |
MOD_CK1_1 | 72 | 78 | PF00069 | 0.749 |
MOD_CK2_1 | 105 | 111 | PF00069 | 0.681 |
MOD_CK2_1 | 259 | 265 | PF00069 | 0.602 |
MOD_CK2_1 | 303 | 309 | PF00069 | 0.819 |
MOD_GlcNHglycan | 239 | 242 | PF01048 | 0.647 |
MOD_GlcNHglycan | 261 | 264 | PF01048 | 0.681 |
MOD_GlcNHglycan | 29 | 32 | PF01048 | 0.534 |
MOD_GlcNHglycan | 298 | 301 | PF01048 | 0.647 |
MOD_GlcNHglycan | 347 | 350 | PF01048 | 0.796 |
MOD_GlcNHglycan | 362 | 365 | PF01048 | 0.523 |
MOD_GlcNHglycan | 382 | 385 | PF01048 | 0.692 |
MOD_GlcNHglycan | 71 | 74 | PF01048 | 0.649 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.615 |
MOD_GSK3_1 | 137 | 144 | PF00069 | 0.481 |
MOD_GSK3_1 | 194 | 201 | PF00069 | 0.645 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.678 |
MOD_GSK3_1 | 27 | 34 | PF00069 | 0.641 |
MOD_GSK3_1 | 348 | 355 | PF00069 | 0.716 |
MOD_GSK3_1 | 375 | 382 | PF00069 | 0.693 |
MOD_GSK3_1 | 44 | 51 | PF00069 | 0.606 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.673 |
MOD_N-GLC_1 | 140 | 145 | PF02516 | 0.490 |
MOD_NEK2_1 | 137 | 142 | PF00069 | 0.537 |
MOD_NEK2_1 | 327 | 332 | PF00069 | 0.534 |
MOD_NEK2_1 | 44 | 49 | PF00069 | 0.632 |
MOD_NEK2_1 | 94 | 99 | PF00069 | 0.742 |
MOD_PIKK_1 | 263 | 269 | PF00454 | 0.693 |
MOD_PIKK_1 | 352 | 358 | PF00454 | 0.790 |
MOD_PIKK_1 | 88 | 94 | PF00454 | 0.644 |
MOD_PKA_1 | 259 | 265 | PF00069 | 0.593 |
MOD_PKA_1 | 271 | 277 | PF00069 | 0.633 |
MOD_PKA_2 | 194 | 200 | PF00069 | 0.721 |
MOD_PKA_2 | 208 | 214 | PF00069 | 0.643 |
MOD_PKA_2 | 270 | 276 | PF00069 | 0.767 |
MOD_PKA_2 | 287 | 293 | PF00069 | 0.546 |
MOD_PKA_2 | 345 | 351 | PF00069 | 0.838 |
MOD_PKA_2 | 36 | 42 | PF00069 | 0.798 |
MOD_PKA_2 | 367 | 373 | PF00069 | 0.734 |
MOD_PKA_2 | 380 | 386 | PF00069 | 0.611 |
MOD_PKA_2 | 78 | 84 | PF00069 | 0.554 |
MOD_PKA_2 | 94 | 100 | PF00069 | 0.779 |
MOD_PKB_1 | 269 | 277 | PF00069 | 0.628 |
MOD_PKB_1 | 366 | 374 | PF00069 | 0.564 |
MOD_Plk_1 | 110 | 116 | PF00069 | 0.780 |
MOD_Plk_2-3 | 110 | 116 | PF00069 | 0.780 |
MOD_Plk_4 | 101 | 107 | PF00069 | 0.549 |
MOD_Plk_4 | 330 | 336 | PF00069 | 0.594 |
MOD_Plk_4 | 36 | 42 | PF00069 | 0.769 |
MOD_ProDKin_1 | 105 | 111 | PF00069 | 0.640 |
MOD_ProDKin_1 | 185 | 191 | PF00069 | 0.780 |
MOD_ProDKin_1 | 198 | 204 | PF00069 | 0.536 |
MOD_ProDKin_1 | 20 | 26 | PF00069 | 0.533 |
MOD_ProDKin_1 | 301 | 307 | PF00069 | 0.825 |
MOD_ProDKin_1 | 348 | 354 | PF00069 | 0.644 |
MOD_ProDKin_1 | 395 | 401 | PF00069 | 0.672 |
MOD_ProDKin_1 | 72 | 78 | PF00069 | 0.565 |
TRG_DiLeu_BaLyEn_6 | 85 | 90 | PF01217 | 0.687 |
TRG_ENDOCYTIC_2 | 404 | 407 | PF00928 | 0.658 |
TRG_ER_diArg_1 | 268 | 271 | PF00400 | 0.762 |
TRG_ER_diArg_1 | 365 | 368 | PF00400 | 0.669 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCW7 | Leptomonas seymouri | 28% | 100% |
A0A3Q8IRH8 | Leishmania donovani | 54% | 95% |
A4I4R7 | Leishmania infantum | 54% | 95% |
E9AE69 | Leishmania major | 53% | 99% |
E9ALL6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 53% | 94% |