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: A0A3S7X356
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 423 | 425 | PF00675 | 0.492 |
CLV_PCSK_KEX2_1 | 423 | 425 | PF00082 | 0.494 |
CLV_PCSK_SKI1_1 | 225 | 229 | PF00082 | 0.689 |
CLV_PCSK_SKI1_1 | 357 | 361 | PF00082 | 0.757 |
CLV_PCSK_SKI1_1 | 452 | 456 | PF00082 | 0.563 |
CLV_PCSK_SKI1_1 | 7 | 11 | PF00082 | 0.498 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.507 |
DEG_SPOP_SBC_1 | 63 | 67 | PF00917 | 0.551 |
DOC_CDC14_PxL_1 | 300 | 308 | PF14671 | 0.539 |
DOC_CKS1_1 | 227 | 232 | PF01111 | 0.650 |
DOC_CKS1_1 | 436 | 441 | PF01111 | 0.662 |
DOC_CYCLIN_RxL_1 | 222 | 229 | PF00134 | 0.753 |
DOC_CYCLIN_yCln2_LP_2 | 12 | 18 | PF00134 | 0.577 |
DOC_CYCLIN_yCln2_LP_2 | 160 | 166 | PF00134 | 0.639 |
DOC_CYCLIN_yCln2_LP_2 | 86 | 92 | PF00134 | 0.663 |
DOC_MAPK_gen_1 | 398 | 408 | PF00069 | 0.621 |
DOC_MAPK_MEF2A_6 | 264 | 273 | PF00069 | 0.757 |
DOC_MAPK_MEF2A_6 | 401 | 408 | PF00069 | 0.607 |
DOC_MAPK_MEF2A_6 | 452 | 460 | PF00069 | 0.553 |
DOC_MAPK_NFAT4_5 | 401 | 409 | PF00069 | 0.570 |
DOC_PP1_RVXF_1 | 237 | 243 | PF00149 | 0.683 |
DOC_PP1_RVXF_1 | 421 | 428 | PF00149 | 0.583 |
DOC_PP4_FxxP_1 | 211 | 214 | PF00568 | 0.755 |
DOC_PP4_FxxP_1 | 301 | 304 | PF00568 | 0.536 |
DOC_SPAK_OSR1_1 | 426 | 430 | PF12202 | 0.673 |
DOC_USP7_MATH_1 | 250 | 254 | PF00917 | 0.697 |
DOC_USP7_MATH_1 | 317 | 321 | PF00917 | 0.699 |
DOC_USP7_MATH_1 | 323 | 327 | PF00917 | 0.702 |
DOC_USP7_MATH_1 | 412 | 416 | PF00917 | 0.739 |
DOC_USP7_MATH_1 | 69 | 73 | PF00917 | 0.615 |
DOC_USP7_UBL2_3 | 127 | 131 | PF12436 | 0.545 |
DOC_WW_Pin1_4 | 197 | 202 | PF00397 | 0.719 |
DOC_WW_Pin1_4 | 210 | 215 | PF00397 | 0.514 |
DOC_WW_Pin1_4 | 226 | 231 | PF00397 | 0.426 |
DOC_WW_Pin1_4 | 31 | 36 | PF00397 | 0.542 |
DOC_WW_Pin1_4 | 319 | 324 | PF00397 | 0.710 |
DOC_WW_Pin1_4 | 370 | 375 | PF00397 | 0.648 |
DOC_WW_Pin1_4 | 415 | 420 | PF00397 | 0.615 |
DOC_WW_Pin1_4 | 435 | 440 | PF00397 | 0.563 |
DOC_WW_Pin1_4 | 65 | 70 | PF00397 | 0.669 |
LIG_14-3-3_CanoR_1 | 264 | 271 | PF00244 | 0.651 |
LIG_BRCT_BRCA1_1 | 205 | 209 | PF00533 | 0.663 |
LIG_CtBP_PxDLS_1 | 89 | 93 | PF00389 | 0.521 |
LIG_FHA_1 | 106 | 112 | PF00498 | 0.639 |
LIG_FHA_1 | 22 | 28 | PF00498 | 0.602 |
LIG_FHA_1 | 358 | 364 | PF00498 | 0.655 |
LIG_FHA_2 | 274 | 280 | PF00498 | 0.723 |
LIG_FHA_2 | 284 | 290 | PF00498 | 0.507 |
LIG_FHA_2 | 371 | 377 | PF00498 | 0.677 |
LIG_LIR_Apic_2 | 37 | 41 | PF02991 | 0.536 |
LIG_LIR_Gen_1 | 219 | 228 | PF02991 | 0.688 |
LIG_LIR_Gen_1 | 338 | 349 | PF02991 | 0.545 |
LIG_LIR_Nem_3 | 135 | 141 | PF02991 | 0.551 |
LIG_LIR_Nem_3 | 219 | 223 | PF02991 | 0.682 |
LIG_LIR_Nem_3 | 25 | 31 | PF02991 | 0.501 |
LIG_LIR_Nem_3 | 254 | 260 | PF02991 | 0.695 |
LIG_LIR_Nem_3 | 338 | 344 | PF02991 | 0.558 |
LIG_NRBOX | 223 | 229 | PF00104 | 0.753 |
LIG_PCNA_yPIPBox_3 | 221 | 231 | PF02747 | 0.628 |
LIG_PDZ_Class_2 | 455 | 460 | PF00595 | 0.647 |
LIG_PTB_Apo_2 | 189 | 196 | PF02174 | 0.737 |
LIG_PTB_Phospho_1 | 189 | 195 | PF10480 | 0.736 |
LIG_SH2_CRK | 134 | 138 | PF00017 | 0.568 |
LIG_SH2_CRK | 205 | 209 | PF00017 | 0.668 |
LIG_SH2_CRK | 220 | 224 | PF00017 | 0.638 |
LIG_SH2_CRK | 341 | 345 | PF00017 | 0.551 |
LIG_SH2_GRB2like | 112 | 115 | PF00017 | 0.566 |
LIG_SH2_GRB2like | 48 | 51 | PF00017 | 0.539 |
LIG_SH2_NCK_1 | 205 | 209 | PF00017 | 0.700 |
LIG_SH2_NCK_1 | 352 | 356 | PF00017 | 0.693 |
LIG_SH2_SRC | 352 | 355 | PF00017 | 0.573 |
LIG_SH2_STAP1 | 134 | 138 | PF00017 | 0.568 |
LIG_SH2_STAP1 | 16 | 20 | PF00017 | 0.585 |
LIG_SH2_STAT5 | 112 | 115 | PF00017 | 0.566 |
LIG_SH2_STAT5 | 134 | 137 | PF00017 | 0.565 |
LIG_SH2_STAT5 | 141 | 144 | PF00017 | 0.535 |
LIG_SH2_STAT5 | 215 | 218 | PF00017 | 0.735 |
LIG_SH2_STAT5 | 236 | 239 | PF00017 | 0.587 |
LIG_SH2_STAT5 | 257 | 260 | PF00017 | 0.700 |
LIG_SH2_STAT5 | 48 | 51 | PF00017 | 0.539 |
LIG_SH3_3 | 371 | 377 | PF00018 | 0.625 |
LIG_SUMO_SIM_par_1 | 87 | 93 | PF11976 | 0.563 |
LIG_TRAF2_1 | 167 | 170 | PF00917 | 0.621 |
LIG_TYR_ITIM | 113 | 118 | PF00017 | 0.554 |
LIG_WRPW_2 | 13 | 16 | PF00400 | 0.682 |
LIG_WRPW_2 | 161 | 164 | PF00400 | 0.599 |
LIG_WW_3 | 354 | 358 | PF00397 | 0.732 |
MOD_CDK_SPK_2 | 226 | 231 | PF00069 | 0.633 |
MOD_CK1_1 | 196 | 202 | PF00069 | 0.684 |
MOD_CK1_1 | 322 | 328 | PF00069 | 0.791 |
MOD_CK1_1 | 415 | 421 | PF00069 | 0.650 |
MOD_CK1_1 | 62 | 68 | PF00069 | 0.710 |
MOD_CK1_1 | 84 | 90 | PF00069 | 0.633 |
MOD_CK2_1 | 273 | 279 | PF00069 | 0.720 |
MOD_CK2_1 | 283 | 289 | PF00069 | 0.484 |
MOD_CK2_1 | 332 | 338 | PF00069 | 0.724 |
MOD_CK2_1 | 370 | 376 | PF00069 | 0.788 |
MOD_CK2_1 | 438 | 444 | PF00069 | 0.580 |
MOD_CMANNOS | 380 | 383 | PF00535 | 0.587 |
MOD_Cter_Amidation | 421 | 424 | PF01082 | 0.576 |
MOD_GlcNHglycan | 149 | 152 | PF01048 | 0.580 |
MOD_GlcNHglycan | 182 | 185 | PF01048 | 0.634 |
MOD_GlcNHglycan | 205 | 208 | PF01048 | 0.767 |
MOD_GlcNHglycan | 254 | 257 | PF01048 | 0.641 |
MOD_GlcNHglycan | 265 | 268 | PF01048 | 0.612 |
MOD_GlcNHglycan | 325 | 328 | PF01048 | 0.751 |
MOD_GlcNHglycan | 329 | 332 | PF01048 | 0.735 |
MOD_GlcNHglycan | 414 | 417 | PF01048 | 0.644 |
MOD_GlcNHglycan | 61 | 64 | PF01048 | 0.735 |
MOD_GlcNHglycan | 71 | 74 | PF01048 | 0.607 |
MOD_GSK3_1 | 193 | 200 | PF00069 | 0.717 |
MOD_GSK3_1 | 27 | 34 | PF00069 | 0.523 |
MOD_GSK3_1 | 271 | 278 | PF00069 | 0.672 |
MOD_GSK3_1 | 317 | 324 | PF00069 | 0.738 |
MOD_GSK3_1 | 434 | 441 | PF00069 | 0.656 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.625 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.581 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.629 |
MOD_LATS_1 | 316 | 322 | PF00433 | 0.619 |
MOD_N-GLC_1 | 139 | 144 | PF02516 | 0.524 |
MOD_N-GLC_2 | 50 | 52 | PF02516 | 0.541 |
MOD_NEK2_1 | 105 | 110 | PF00069 | 0.513 |
MOD_NEK2_1 | 182 | 187 | PF00069 | 0.697 |
MOD_NEK2_1 | 209 | 214 | PF00069 | 0.738 |
MOD_NEK2_1 | 271 | 276 | PF00069 | 0.780 |
MOD_NEK2_1 | 344 | 349 | PF00069 | 0.509 |
MOD_NEK2_1 | 369 | 374 | PF00069 | 0.796 |
MOD_NEK2_1 | 61 | 66 | PF00069 | 0.737 |
MOD_NEK2_1 | 77 | 82 | PF00069 | 0.597 |
MOD_NEK2_1 | 90 | 95 | PF00069 | 0.529 |
MOD_NEK2_2 | 139 | 144 | PF00069 | 0.557 |
MOD_PIKK_1 | 22 | 28 | PF00454 | 0.508 |
MOD_PKA_2 | 263 | 269 | PF00069 | 0.654 |
MOD_PKA_2 | 317 | 323 | PF00069 | 0.609 |
MOD_Plk_1 | 139 | 145 | PF00069 | 0.488 |
MOD_Plk_1 | 22 | 28 | PF00069 | 0.536 |
MOD_Plk_1 | 337 | 343 | PF00069 | 0.678 |
MOD_Plk_1 | 90 | 96 | PF00069 | 0.504 |
MOD_Plk_4 | 132 | 138 | PF00069 | 0.557 |
MOD_Plk_4 | 139 | 145 | PF00069 | 0.510 |
MOD_Plk_4 | 34 | 40 | PF00069 | 0.635 |
MOD_Plk_4 | 438 | 444 | PF00069 | 0.580 |
MOD_Plk_4 | 81 | 87 | PF00069 | 0.629 |
MOD_ProDKin_1 | 197 | 203 | PF00069 | 0.721 |
MOD_ProDKin_1 | 210 | 216 | PF00069 | 0.512 |
MOD_ProDKin_1 | 226 | 232 | PF00069 | 0.422 |
MOD_ProDKin_1 | 31 | 37 | PF00069 | 0.541 |
MOD_ProDKin_1 | 319 | 325 | PF00069 | 0.706 |
MOD_ProDKin_1 | 370 | 376 | PF00069 | 0.644 |
MOD_ProDKin_1 | 415 | 421 | PF00069 | 0.617 |
MOD_ProDKin_1 | 435 | 441 | PF00069 | 0.570 |
MOD_ProDKin_1 | 65 | 71 | PF00069 | 0.669 |
MOD_SUMO_rev_2 | 119 | 129 | PF00179 | 0.649 |
TRG_DiLeu_BaEn_1 | 219 | 224 | PF01217 | 0.739 |
TRG_DiLeu_BaLyEn_6 | 365 | 370 | PF01217 | 0.707 |
TRG_ENDOCYTIC_2 | 115 | 118 | PF00928 | 0.551 |
TRG_ENDOCYTIC_2 | 134 | 137 | PF00928 | 0.565 |
TRG_ENDOCYTIC_2 | 161 | 164 | PF00928 | 0.550 |
TRG_ENDOCYTIC_2 | 220 | 223 | PF00928 | 0.629 |
TRG_ENDOCYTIC_2 | 341 | 344 | PF00928 | 0.532 |
TRG_ER_diArg_1 | 423 | 426 | PF00400 | 0.499 |
TRG_Pf-PMV_PEXEL_1 | 7 | 11 | PF00026 | 0.611 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8W7 | Leptomonas seymouri | 57% | 86% |
A4HI53 | Leishmania braziliensis | 84% | 100% |
A4I5C9 | Leishmania infantum | 100% | 100% |
E9B0M7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
Q4Q7K5 | Leishmania major | 94% | 100% |