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: A0A3Q8IJX1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 166 | 168 | PF00675 | 0.648 |
CLV_NRD_NRD_1 | 228 | 230 | PF00675 | 0.461 |
CLV_NRD_NRD_1 | 40 | 42 | PF00675 | 0.460 |
CLV_NRD_NRD_1 | 79 | 81 | PF00675 | 0.634 |
CLV_PCSK_KEX2_1 | 166 | 168 | PF00082 | 0.724 |
CLV_PCSK_KEX2_1 | 228 | 230 | PF00082 | 0.461 |
CLV_PCSK_KEX2_1 | 238 | 240 | PF00082 | 0.519 |
CLV_PCSK_KEX2_1 | 353 | 355 | PF00082 | 0.441 |
CLV_PCSK_KEX2_1 | 39 | 41 | PF00082 | 0.457 |
CLV_PCSK_KEX2_1 | 79 | 81 | PF00082 | 0.625 |
CLV_PCSK_PC1ET2_1 | 238 | 240 | PF00082 | 0.519 |
CLV_PCSK_PC1ET2_1 | 353 | 355 | PF00082 | 0.441 |
CLV_PCSK_PC1ET2_1 | 39 | 41 | PF00082 | 0.447 |
CLV_PCSK_SKI1_1 | 257 | 261 | PF00082 | 0.423 |
CLV_PCSK_SKI1_1 | 302 | 306 | PF00082 | 0.415 |
CLV_PCSK_SKI1_1 | 353 | 357 | PF00082 | 0.454 |
DEG_ODPH_VHL_1 | 271 | 283 | PF01847 | 0.443 |
DEG_SPOP_SBC_1 | 62 | 66 | PF00917 | 0.633 |
DOC_CYCLIN_yCln2_LP_2 | 240 | 246 | PF00134 | 0.517 |
DOC_CYCLIN_yCln2_LP_2 | 54 | 60 | PF00134 | 0.546 |
DOC_MAPK_gen_1 | 39 | 48 | PF00069 | 0.525 |
DOC_MAPK_MEF2A_6 | 29 | 37 | PF00069 | 0.520 |
DOC_PP2B_LxvP_1 | 252 | 255 | PF13499 | 0.453 |
DOC_PP2B_LxvP_1 | 54 | 57 | PF13499 | 0.563 |
DOC_PP4_FxxP_1 | 346 | 349 | PF00568 | 0.343 |
DOC_USP7_MATH_1 | 128 | 132 | PF00917 | 0.532 |
DOC_USP7_MATH_1 | 160 | 164 | PF00917 | 0.633 |
DOC_USP7_MATH_1 | 169 | 173 | PF00917 | 0.714 |
DOC_USP7_MATH_1 | 215 | 219 | PF00917 | 0.504 |
DOC_USP7_MATH_1 | 246 | 250 | PF00917 | 0.526 |
DOC_USP7_MATH_1 | 62 | 66 | PF00917 | 0.754 |
DOC_USP7_UBL2_3 | 238 | 242 | PF12436 | 0.519 |
DOC_USP7_UBL2_3 | 298 | 302 | PF12436 | 0.456 |
DOC_WW_Pin1_4 | 150 | 155 | PF00397 | 0.672 |
DOC_WW_Pin1_4 | 167 | 172 | PF00397 | 0.550 |
DOC_WW_Pin1_4 | 179 | 184 | PF00397 | 0.638 |
DOC_WW_Pin1_4 | 213 | 218 | PF00397 | 0.571 |
DOC_WW_Pin1_4 | 359 | 364 | PF00397 | 0.575 |
DOC_WW_Pin1_4 | 86 | 91 | PF00397 | 0.697 |
LIG_14-3-3_CanoR_1 | 102 | 108 | PF00244 | 0.627 |
LIG_14-3-3_CanoR_1 | 129 | 138 | PF00244 | 0.531 |
LIG_14-3-3_CanoR_1 | 141 | 149 | PF00244 | 0.627 |
LIG_14-3-3_CanoR_1 | 232 | 240 | PF00244 | 0.510 |
LIG_14-3-3_CanoR_1 | 91 | 97 | PF00244 | 0.553 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.628 |
LIG_BIR_III_4 | 6 | 10 | PF00653 | 0.478 |
LIG_eIF4E_1 | 21 | 27 | PF01652 | 0.472 |
LIG_FHA_1 | 303 | 309 | PF00498 | 0.377 |
LIG_FHA_1 | 49 | 55 | PF00498 | 0.501 |
LIG_FHA_1 | 62 | 68 | PF00498 | 0.683 |
LIG_FHA_2 | 10 | 16 | PF00498 | 0.574 |
LIG_FHA_2 | 130 | 136 | PF00498 | 0.571 |
LIG_FHA_2 | 214 | 220 | PF00498 | 0.547 |
LIG_FHA_2 | 283 | 289 | PF00498 | 0.374 |
LIG_IRF3_LxIS_1 | 184 | 191 | PF10401 | 0.597 |
LIG_LIR_Apic_2 | 345 | 349 | PF02991 | 0.341 |
LIG_LIR_Gen_1 | 28 | 37 | PF02991 | 0.471 |
LIG_LIR_Gen_1 | 330 | 339 | PF02991 | 0.394 |
LIG_LIR_Nem_3 | 28 | 33 | PF02991 | 0.530 |
LIG_LIR_Nem_3 | 330 | 336 | PF02991 | 0.387 |
LIG_LIR_Nem_3 | 42 | 48 | PF02991 | 0.452 |
LIG_Pex14_2 | 346 | 350 | PF04695 | 0.346 |
LIG_SH2_CRK | 204 | 208 | PF00017 | 0.516 |
LIG_SH2_CRK | 268 | 272 | PF00017 | 0.361 |
LIG_SH2_CRK | 30 | 34 | PF00017 | 0.430 |
LIG_SH2_CRK | 58 | 62 | PF00017 | 0.559 |
LIG_SH2_GRB2like | 310 | 313 | PF00017 | 0.366 |
LIG_SH2_NCK_1 | 221 | 225 | PF00017 | 0.562 |
LIG_SH2_SRC | 21 | 24 | PF00017 | 0.510 |
LIG_SH2_STAP1 | 17 | 21 | PF00017 | 0.545 |
LIG_SH2_STAP1 | 221 | 225 | PF00017 | 0.562 |
LIG_SH2_STAP1 | 58 | 62 | PF00017 | 0.583 |
LIG_SH2_STAT5 | 21 | 24 | PF00017 | 0.487 |
LIG_SH2_STAT5 | 293 | 296 | PF00017 | 0.385 |
LIG_SH2_STAT5 | 344 | 347 | PF00017 | 0.340 |
LIG_SH3_3 | 214 | 220 | PF00018 | 0.560 |
LIG_SH3_3 | 240 | 246 | PF00018 | 0.517 |
LIG_SH3_3 | 274 | 280 | PF00018 | 0.447 |
LIG_SH3_3 | 358 | 364 | PF00018 | 0.530 |
LIG_SUMO_SIM_par_1 | 279 | 285 | PF11976 | 0.445 |
LIG_TYR_ITIM | 56 | 61 | PF00017 | 0.574 |
LIG_UBA3_1 | 307 | 316 | PF00899 | 0.445 |
LIG_WRC_WIRS_1 | 343 | 348 | PF05994 | 0.332 |
MOD_CDK_SPK_2 | 86 | 91 | PF00069 | 0.621 |
MOD_CK1_1 | 103 | 109 | PF00069 | 0.692 |
MOD_CK1_1 | 172 | 178 | PF00069 | 0.687 |
MOD_CK1_1 | 49 | 55 | PF00069 | 0.574 |
MOD_CK1_1 | 75 | 81 | PF00069 | 0.647 |
MOD_CK1_1 | 89 | 95 | PF00069 | 0.545 |
MOD_CK2_1 | 129 | 135 | PF00069 | 0.585 |
MOD_CK2_1 | 281 | 287 | PF00069 | 0.382 |
MOD_CK2_1 | 324 | 330 | PF00069 | 0.401 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.585 |
MOD_GlcNHglycan | 109 | 112 | PF01048 | 0.679 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.658 |
MOD_GlcNHglycan | 163 | 166 | PF01048 | 0.656 |
MOD_GlcNHglycan | 171 | 174 | PF01048 | 0.731 |
MOD_GlcNHglycan | 190 | 193 | PF01048 | 0.609 |
MOD_GlcNHglycan | 246 | 249 | PF01048 | 0.530 |
MOD_GlcNHglycan | 51 | 54 | PF01048 | 0.534 |
MOD_GlcNHglycan | 74 | 77 | PF01048 | 0.588 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.630 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.627 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.668 |
MOD_GSK3_1 | 203 | 210 | PF00069 | 0.556 |
MOD_GSK3_1 | 44 | 51 | PF00069 | 0.455 |
MOD_GSK3_1 | 68 | 75 | PF00069 | 0.578 |
MOD_N-GLC_2 | 124 | 126 | PF02516 | 0.610 |
MOD_N-GLC_2 | 312 | 314 | PF02516 | 0.394 |
MOD_NEK2_1 | 100 | 105 | PF00069 | 0.720 |
MOD_NEK2_1 | 107 | 112 | PF00069 | 0.614 |
MOD_NEK2_1 | 155 | 160 | PF00069 | 0.592 |
MOD_NEK2_1 | 207 | 212 | PF00069 | 0.481 |
MOD_NEK2_1 | 234 | 239 | PF00069 | 0.515 |
MOD_NEK2_1 | 267 | 272 | PF00069 | 0.355 |
MOD_NEK2_1 | 324 | 329 | PF00069 | 0.441 |
MOD_NEK2_1 | 46 | 51 | PF00069 | 0.467 |
MOD_NEK2_1 | 61 | 66 | PF00069 | 0.529 |
MOD_NEK2_2 | 9 | 14 | PF00069 | 0.555 |
MOD_PIKK_1 | 46 | 52 | PF00454 | 0.517 |
MOD_PKA_2 | 103 | 109 | PF00069 | 0.610 |
MOD_PKA_2 | 128 | 134 | PF00069 | 0.508 |
MOD_PKA_2 | 160 | 166 | PF00069 | 0.712 |
MOD_Plk_1 | 322 | 328 | PF00069 | 0.438 |
MOD_Plk_2-3 | 334 | 340 | PF00069 | 0.418 |
MOD_ProDKin_1 | 150 | 156 | PF00069 | 0.674 |
MOD_ProDKin_1 | 167 | 173 | PF00069 | 0.551 |
MOD_ProDKin_1 | 179 | 185 | PF00069 | 0.640 |
MOD_ProDKin_1 | 213 | 219 | PF00069 | 0.566 |
MOD_ProDKin_1 | 359 | 365 | PF00069 | 0.576 |
MOD_ProDKin_1 | 86 | 92 | PF00069 | 0.695 |
MOD_SUMO_rev_2 | 231 | 240 | PF00179 | 0.480 |
TRG_ENDOCYTIC_2 | 10 | 13 | PF00928 | 0.622 |
TRG_ENDOCYTIC_2 | 204 | 207 | PF00928 | 0.516 |
TRG_ENDOCYTIC_2 | 268 | 271 | PF00928 | 0.366 |
TRG_ENDOCYTIC_2 | 293 | 296 | PF00928 | 0.352 |
TRG_ENDOCYTIC_2 | 30 | 33 | PF00928 | 0.421 |
TRG_ENDOCYTIC_2 | 58 | 61 | PF00928 | 0.582 |
TRG_ER_diArg_1 | 140 | 143 | PF00400 | 0.573 |
TRG_ER_diArg_1 | 195 | 198 | PF00400 | 0.703 |
TRG_NLS_MonoExtN_4 | 349 | 356 | PF00514 | 0.412 |
TRG_Pf-PMV_PEXEL_1 | 232 | 236 | PF00026 | 0.492 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P717 | Leptomonas seymouri | 52% | 100% |
A4HL74 | Leishmania braziliensis | 67% | 100% |
A4I8Q3 | Leishmania infantum | 100% | 100% |
E9B3L7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
Q4Q4G8 | Leishmania major | 90% | 100% |