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: A4ICK4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 383 | 387 | PF00656 | 0.514 |
CLV_MEL_PAP_1 | 133 | 139 | PF00089 | 0.523 |
CLV_NRD_NRD_1 | 146 | 148 | PF00675 | 0.488 |
CLV_NRD_NRD_1 | 151 | 153 | PF00675 | 0.489 |
CLV_NRD_NRD_1 | 17 | 19 | PF00675 | 0.694 |
CLV_NRD_NRD_1 | 206 | 208 | PF00675 | 0.607 |
CLV_NRD_NRD_1 | 233 | 235 | PF00675 | 0.616 |
CLV_NRD_NRD_1 | 342 | 344 | PF00675 | 0.628 |
CLV_NRD_NRD_1 | 80 | 82 | PF00675 | 0.627 |
CLV_PCSK_KEX2_1 | 145 | 147 | PF00082 | 0.496 |
CLV_PCSK_KEX2_1 | 17 | 19 | PF00082 | 0.694 |
CLV_PCSK_KEX2_1 | 206 | 208 | PF00082 | 0.584 |
CLV_PCSK_KEX2_1 | 233 | 235 | PF00082 | 0.571 |
CLV_PCSK_KEX2_1 | 342 | 344 | PF00082 | 0.611 |
CLV_PCSK_KEX2_1 | 80 | 82 | PF00082 | 0.769 |
CLV_PCSK_PC1ET2_1 | 342 | 344 | PF00082 | 0.611 |
CLV_PCSK_SKI1_1 | 185 | 189 | PF00082 | 0.443 |
DEG_SPOP_SBC_1 | 295 | 299 | PF00917 | 0.616 |
DEG_SPOP_SBC_1 | 306 | 310 | PF00917 | 0.520 |
DOC_CKS1_1 | 86 | 91 | PF01111 | 0.637 |
DOC_CKS1_1 | 92 | 97 | PF01111 | 0.552 |
DOC_MAPK_gen_1 | 152 | 160 | PF00069 | 0.455 |
DOC_MAPK_gen_1 | 17 | 27 | PF00069 | 0.611 |
DOC_MAPK_MEF2A_6 | 153 | 162 | PF00069 | 0.367 |
DOC_MAPK_RevD_3 | 133 | 146 | PF00069 | 0.445 |
DOC_PP1_RVXF_1 | 191 | 197 | PF00149 | 0.412 |
DOC_USP7_MATH_1 | 295 | 299 | PF00917 | 0.665 |
DOC_USP7_MATH_1 | 38 | 42 | PF00917 | 0.626 |
DOC_USP7_MATH_1 | 397 | 401 | PF00917 | 0.590 |
DOC_USP7_MATH_1 | 55 | 59 | PF00917 | 0.586 |
DOC_USP7_MATH_1 | 8 | 12 | PF00917 | 0.560 |
DOC_USP7_UBL2_3 | 36 | 40 | PF12436 | 0.643 |
DOC_WW_Pin1_4 | 205 | 210 | PF00397 | 0.509 |
DOC_WW_Pin1_4 | 248 | 253 | PF00397 | 0.446 |
DOC_WW_Pin1_4 | 332 | 337 | PF00397 | 0.611 |
DOC_WW_Pin1_4 | 356 | 361 | PF00397 | 0.678 |
DOC_WW_Pin1_4 | 56 | 61 | PF00397 | 0.707 |
DOC_WW_Pin1_4 | 79 | 84 | PF00397 | 0.711 |
DOC_WW_Pin1_4 | 85 | 90 | PF00397 | 0.650 |
DOC_WW_Pin1_4 | 91 | 96 | PF00397 | 0.551 |
DOC_WW_Pin1_4 | 99 | 104 | PF00397 | 0.642 |
LIG_14-3-3_CanoR_1 | 136 | 142 | PF00244 | 0.587 |
LIG_14-3-3_CanoR_1 | 17 | 27 | PF00244 | 0.638 |
LIG_14-3-3_CanoR_1 | 185 | 191 | PF00244 | 0.443 |
LIG_14-3-3_CanoR_1 | 218 | 224 | PF00244 | 0.476 |
LIG_14-3-3_CanoR_1 | 233 | 241 | PF00244 | 0.389 |
LIG_14-3-3_CanoR_1 | 259 | 268 | PF00244 | 0.523 |
LIG_14-3-3_CanoR_1 | 30 | 38 | PF00244 | 0.587 |
LIG_14-3-3_CanoR_1 | 305 | 314 | PF00244 | 0.698 |
LIG_14-3-3_CanoR_1 | 343 | 349 | PF00244 | 0.694 |
LIG_14-3-3_CanoR_1 | 61 | 65 | PF00244 | 0.617 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.542 |
LIG_BIR_III_2 | 285 | 289 | PF00653 | 0.618 |
LIG_FHA_1 | 261 | 267 | PF00498 | 0.426 |
LIG_FHA_1 | 307 | 313 | PF00498 | 0.622 |
LIG_FHA_1 | 66 | 72 | PF00498 | 0.631 |
LIG_FHA_1 | 80 | 86 | PF00498 | 0.612 |
LIG_FHA_2 | 235 | 241 | PF00498 | 0.536 |
LIG_FHA_2 | 365 | 371 | PF00498 | 0.702 |
LIG_FHA_2 | 381 | 387 | PF00498 | 0.460 |
LIG_FHA_2 | 46 | 52 | PF00498 | 0.722 |
LIG_FHA_2 | 86 | 92 | PF00498 | 0.599 |
LIG_LIR_Gen_1 | 245 | 255 | PF02991 | 0.536 |
LIG_LIR_Gen_1 | 45 | 55 | PF02991 | 0.562 |
LIG_LIR_Gen_1 | 5 | 12 | PF02991 | 0.529 |
LIG_LIR_Gen_1 | 59 | 69 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 231 | 235 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 245 | 250 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 45 | 50 | PF02991 | 0.576 |
LIG_LIR_Nem_3 | 5 | 9 | PF02991 | 0.637 |
LIG_LIR_Nem_3 | 59 | 65 | PF02991 | 0.630 |
LIG_PDZ_Class_2 | 417 | 422 | PF00595 | 0.461 |
LIG_SH2_NCK_1 | 406 | 410 | PF00017 | 0.419 |
LIG_SH2_NCK_1 | 47 | 51 | PF00017 | 0.600 |
LIG_SH2_SRC | 406 | 409 | PF00017 | 0.425 |
LIG_SH2_STAP1 | 23 | 27 | PF00017 | 0.666 |
LIG_SH2_STAP1 | 406 | 410 | PF00017 | 0.438 |
LIG_SH2_STAT5 | 47 | 50 | PF00017 | 0.602 |
LIG_SH3_3 | 287 | 293 | PF00018 | 0.650 |
LIG_SH3_3 | 68 | 74 | PF00018 | 0.663 |
LIG_SH3_5 | 19 | 23 | PF00018 | 0.526 |
LIG_TRAF2_1 | 163 | 166 | PF00917 | 0.359 |
LIG_WW_3 | 102 | 106 | PF00397 | 0.514 |
MOD_CDK_SPK_2 | 56 | 61 | PF00069 | 0.605 |
MOD_CDK_SPK_2 | 85 | 90 | PF00069 | 0.621 |
MOD_CDK_SPxK_1 | 99 | 105 | PF00069 | 0.521 |
MOD_CDK_SPxxK_3 | 356 | 363 | PF00069 | 0.565 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.610 |
MOD_CK1_1 | 21 | 27 | PF00069 | 0.490 |
MOD_CK1_1 | 236 | 242 | PF00069 | 0.485 |
MOD_CK1_1 | 260 | 266 | PF00069 | 0.429 |
MOD_CK1_1 | 308 | 314 | PF00069 | 0.618 |
MOD_CK1_1 | 395 | 401 | PF00069 | 0.516 |
MOD_CK1_1 | 411 | 417 | PF00069 | 0.434 |
MOD_CK1_1 | 43 | 49 | PF00069 | 0.715 |
MOD_CK2_1 | 234 | 240 | PF00069 | 0.629 |
MOD_CK2_1 | 356 | 362 | PF00069 | 0.683 |
MOD_CK2_1 | 364 | 370 | PF00069 | 0.638 |
MOD_CK2_1 | 401 | 407 | PF00069 | 0.594 |
MOD_CK2_1 | 45 | 51 | PF00069 | 0.683 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.551 |
MOD_GlcNHglycan | 214 | 217 | PF01048 | 0.584 |
MOD_GlcNHglycan | 219 | 222 | PF01048 | 0.464 |
MOD_GlcNHglycan | 244 | 247 | PF01048 | 0.532 |
MOD_GlcNHglycan | 302 | 305 | PF01048 | 0.675 |
MOD_GlcNHglycan | 318 | 321 | PF01048 | 0.501 |
MOD_GlcNHglycan | 396 | 400 | PF01048 | 0.485 |
MOD_GlcNHglycan | 42 | 45 | PF01048 | 0.645 |
MOD_GSK3_1 | 108 | 115 | PF00069 | 0.606 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.480 |
MOD_GSK3_1 | 296 | 303 | PF00069 | 0.634 |
MOD_GSK3_1 | 304 | 311 | PF00069 | 0.684 |
MOD_GSK3_1 | 38 | 45 | PF00069 | 0.668 |
MOD_GSK3_1 | 397 | 404 | PF00069 | 0.595 |
MOD_GSK3_1 | 56 | 63 | PF00069 | 0.669 |
MOD_GSK3_1 | 99 | 106 | PF00069 | 0.700 |
MOD_N-GLC_1 | 280 | 285 | PF02516 | 0.524 |
MOD_N-GLC_1 | 316 | 321 | PF02516 | 0.657 |
MOD_N-GLC_1 | 356 | 361 | PF02516 | 0.647 |
MOD_NEK2_1 | 186 | 191 | PF00069 | 0.390 |
MOD_NEK2_1 | 300 | 305 | PF00069 | 0.640 |
MOD_NEK2_1 | 316 | 321 | PF00069 | 0.504 |
MOD_NEK2_2 | 296 | 301 | PF00069 | 0.550 |
MOD_PIKK_1 | 260 | 266 | PF00454 | 0.429 |
MOD_PK_1 | 344 | 350 | PF00069 | 0.534 |
MOD_PKA_1 | 233 | 239 | PF00069 | 0.524 |
MOD_PKA_1 | 344 | 350 | PF00069 | 0.611 |
MOD_PKA_2 | 135 | 141 | PF00069 | 0.580 |
MOD_PKA_2 | 217 | 223 | PF00069 | 0.480 |
MOD_PKA_2 | 233 | 239 | PF00069 | 0.441 |
MOD_PKA_2 | 300 | 306 | PF00069 | 0.655 |
MOD_PKA_2 | 60 | 66 | PF00069 | 0.604 |
MOD_Plk_1 | 181 | 187 | PF00069 | 0.552 |
MOD_Plk_1 | 21 | 27 | PF00069 | 0.458 |
MOD_Plk_4 | 308 | 314 | PF00069 | 0.680 |
MOD_Plk_4 | 344 | 350 | PF00069 | 0.613 |
MOD_Plk_4 | 401 | 407 | PF00069 | 0.526 |
MOD_Plk_4 | 408 | 414 | PF00069 | 0.441 |
MOD_ProDKin_1 | 205 | 211 | PF00069 | 0.507 |
MOD_ProDKin_1 | 248 | 254 | PF00069 | 0.460 |
MOD_ProDKin_1 | 332 | 338 | PF00069 | 0.609 |
MOD_ProDKin_1 | 356 | 362 | PF00069 | 0.683 |
MOD_ProDKin_1 | 56 | 62 | PF00069 | 0.710 |
MOD_ProDKin_1 | 79 | 85 | PF00069 | 0.712 |
MOD_ProDKin_1 | 91 | 97 | PF00069 | 0.552 |
MOD_ProDKin_1 | 99 | 105 | PF00069 | 0.643 |
MOD_SUMO_rev_2 | 28 | 38 | PF00179 | 0.478 |
TRG_DiLeu_BaEn_1 | 182 | 187 | PF01217 | 0.470 |
TRG_DiLeu_LyEn_5 | 182 | 187 | PF01217 | 0.444 |
TRG_ENDOCYTIC_2 | 47 | 50 | PF00928 | 0.574 |
TRG_ENDOCYTIC_2 | 6 | 9 | PF00928 | 0.640 |
TRG_ER_diArg_1 | 145 | 147 | PF00400 | 0.632 |
TRG_ER_diArg_1 | 16 | 18 | PF00400 | 0.659 |
TRG_ER_diArg_1 | 232 | 234 | PF00400 | 0.557 |
TRG_ER_diArg_1 | 416 | 419 | PF00400 | 0.445 |
TRG_NLS_MonoExtN_4 | 342 | 347 | PF00514 | 0.610 |
TRG_Pf-PMV_PEXEL_1 | 259 | 264 | PF00026 | 0.431 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZ64 | Leptomonas seymouri | 32% | 100% |
A0A3S7XAJ3 | Leishmania donovani | 99% | 100% |
A4HNY9 | Leishmania braziliensis | 58% | 100% |
E9ASQ1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 77% | 100% |
Q4Q1U4 | Leishmania major | 83% | 100% |