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: E9B671
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 110 | 112 | PF00675 | 0.696 |
CLV_NRD_NRD_1 | 438 | 440 | PF00675 | 0.672 |
CLV_PCSK_FUR_1 | 108 | 112 | PF00082 | 0.633 |
CLV_PCSK_KEX2_1 | 110 | 112 | PF00082 | 0.696 |
CLV_Separin_Metazoa | 187 | 191 | PF03568 | 0.470 |
CLV_Separin_Metazoa | 317 | 321 | PF03568 | 0.503 |
DEG_APCC_KENBOX_2 | 409 | 413 | PF00400 | 0.643 |
DEG_SPOP_SBC_1 | 83 | 87 | PF00917 | 0.415 |
DOC_PP2B_LxvP_1 | 135 | 138 | PF13499 | 0.664 |
DOC_PP2B_LxvP_1 | 97 | 100 | PF13499 | 0.634 |
DOC_PP4_FxxP_1 | 271 | 274 | PF00568 | 0.503 |
DOC_PP4_FxxP_1 | 341 | 344 | PF00568 | 0.514 |
DOC_PP4_FxxP_1 | 346 | 349 | PF00568 | 0.469 |
DOC_USP7_MATH_1 | 152 | 156 | PF00917 | 0.506 |
DOC_USP7_MATH_1 | 162 | 166 | PF00917 | 0.433 |
DOC_USP7_MATH_1 | 243 | 247 | PF00917 | 0.758 |
DOC_USP7_MATH_1 | 249 | 253 | PF00917 | 0.668 |
DOC_USP7_MATH_1 | 263 | 267 | PF00917 | 0.675 |
DOC_USP7_MATH_1 | 296 | 300 | PF00917 | 0.585 |
DOC_USP7_MATH_1 | 385 | 389 | PF00917 | 0.381 |
DOC_USP7_MATH_1 | 59 | 63 | PF00917 | 0.553 |
DOC_USP7_MATH_1 | 83 | 87 | PF00917 | 0.642 |
DOC_USP7_MATH_1 | 88 | 92 | PF00917 | 0.624 |
DOC_WW_Pin1_4 | 125 | 130 | PF00397 | 0.636 |
DOC_WW_Pin1_4 | 141 | 146 | PF00397 | 0.727 |
DOC_WW_Pin1_4 | 148 | 153 | PF00397 | 0.609 |
DOC_WW_Pin1_4 | 156 | 161 | PF00397 | 0.443 |
DOC_WW_Pin1_4 | 245 | 250 | PF00397 | 0.666 |
DOC_WW_Pin1_4 | 26 | 31 | PF00397 | 0.487 |
DOC_WW_Pin1_4 | 272 | 277 | PF00397 | 0.756 |
DOC_WW_Pin1_4 | 281 | 286 | PF00397 | 0.645 |
DOC_WW_Pin1_4 | 365 | 370 | PF00397 | 0.449 |
LIG_14-3-3_CanoR_1 | 381 | 385 | PF00244 | 0.497 |
LIG_14-3-3_CanoR_1 | 63 | 73 | PF00244 | 0.521 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.578 |
LIG_BIR_III_4 | 58 | 62 | PF00653 | 0.543 |
LIG_BRCT_BRCA1_1 | 413 | 417 | PF00533 | 0.534 |
LIG_deltaCOP1_diTrp_1 | 328 | 334 | PF00928 | 0.396 |
LIG_FHA_1 | 10 | 16 | PF00498 | 0.611 |
LIG_FHA_1 | 381 | 387 | PF00498 | 0.409 |
LIG_FHA_1 | 432 | 438 | PF00498 | 0.576 |
LIG_FHA_1 | 94 | 100 | PF00498 | 0.745 |
LIG_FHA_2 | 113 | 119 | PF00498 | 0.602 |
LIG_FHA_2 | 27 | 33 | PF00498 | 0.461 |
LIG_LIR_Apic_2 | 270 | 274 | PF02991 | 0.501 |
LIG_LIR_Apic_2 | 398 | 403 | PF02991 | 0.592 |
LIG_LIR_Gen_1 | 76 | 84 | PF02991 | 0.499 |
LIG_LIR_Nem_3 | 171 | 177 | PF02991 | 0.481 |
LIG_LIR_Nem_3 | 245 | 250 | PF02991 | 0.619 |
LIG_LIR_Nem_3 | 328 | 333 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 76 | 82 | PF02991 | 0.483 |
LIG_MAD2 | 424 | 432 | PF02301 | 0.564 |
LIG_PDZ_Class_2 | 444 | 449 | PF00595 | 0.663 |
LIG_Pex14_1 | 330 | 334 | PF04695 | 0.397 |
LIG_Pex14_2 | 206 | 210 | PF04695 | 0.437 |
LIG_PTB_Apo_2 | 188 | 195 | PF02174 | 0.475 |
LIG_SH2_CRK | 247 | 251 | PF00017 | 0.622 |
LIG_SH2_CRK | 322 | 326 | PF00017 | 0.390 |
LIG_SH2_GRB2like | 73 | 76 | PF00017 | 0.576 |
LIG_SH2_NCK_1 | 79 | 83 | PF00017 | 0.570 |
LIG_SH2_SRC | 79 | 82 | PF00017 | 0.506 |
LIG_SH2_STAP1 | 73 | 77 | PF00017 | 0.492 |
LIG_SH2_STAP1 | 79 | 83 | PF00017 | 0.496 |
LIG_SH2_STAT3 | 333 | 336 | PF00017 | 0.401 |
LIG_SH2_STAT5 | 114 | 117 | PF00017 | 0.691 |
LIG_SH2_STAT5 | 177 | 180 | PF00017 | 0.461 |
LIG_SH2_STAT5 | 333 | 336 | PF00017 | 0.401 |
LIG_SH2_STAT5 | 377 | 380 | PF00017 | 0.439 |
LIG_SH2_STAT5 | 39 | 42 | PF00017 | 0.461 |
LIG_SH3_3 | 140 | 146 | PF00018 | 0.689 |
LIG_SH3_3 | 271 | 277 | PF00018 | 0.668 |
LIG_SH3_3 | 282 | 288 | PF00018 | 0.634 |
LIG_SH3_3 | 387 | 393 | PF00018 | 0.399 |
LIG_TRAF2_1 | 237 | 240 | PF00917 | 0.627 |
LIG_WRC_WIRS_1 | 5 | 10 | PF05994 | 0.577 |
MOD_CDC14_SPxK_1 | 248 | 251 | PF00782 | 0.667 |
MOD_CDK_SPxK_1 | 245 | 251 | PF00069 | 0.677 |
MOD_CK1_1 | 139 | 145 | PF00069 | 0.687 |
MOD_CK1_1 | 148 | 154 | PF00069 | 0.587 |
MOD_CK1_1 | 216 | 222 | PF00069 | 0.360 |
MOD_CK1_1 | 245 | 251 | PF00069 | 0.535 |
MOD_CK1_1 | 254 | 260 | PF00069 | 0.502 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.474 |
MOD_CK2_1 | 112 | 118 | PF00069 | 0.597 |
MOD_GlcNHglycan | 103 | 106 | PF01048 | 0.748 |
MOD_GlcNHglycan | 138 | 141 | PF01048 | 0.686 |
MOD_GlcNHglycan | 164 | 167 | PF01048 | 0.543 |
MOD_GlcNHglycan | 218 | 221 | PF01048 | 0.420 |
MOD_GlcNHglycan | 253 | 256 | PF01048 | 0.652 |
MOD_GlcNHglycan | 299 | 302 | PF01048 | 0.494 |
MOD_GlcNHglycan | 31 | 36 | PF01048 | 0.724 |
MOD_GlcNHglycan | 359 | 362 | PF01048 | 0.636 |
MOD_GlcNHglycan | 387 | 390 | PF01048 | 0.383 |
MOD_GlcNHglycan | 9 | 12 | PF01048 | 0.469 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.635 |
MOD_GSK3_1 | 141 | 148 | PF00069 | 0.698 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.513 |
MOD_GSK3_1 | 194 | 201 | PF00069 | 0.483 |
MOD_GSK3_1 | 245 | 252 | PF00069 | 0.616 |
MOD_GSK3_1 | 263 | 270 | PF00069 | 0.573 |
MOD_GSK3_1 | 277 | 284 | PF00069 | 0.664 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.522 |
MOD_GSK3_1 | 83 | 90 | PF00069 | 0.627 |
MOD_N-GLC_1 | 194 | 199 | PF02516 | 0.477 |
MOD_N-GLC_1 | 297 | 302 | PF02516 | 0.455 |
MOD_N-GLC_1 | 411 | 416 | PF02516 | 0.554 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.576 |
MOD_NEK2_1 | 194 | 199 | PF00069 | 0.477 |
MOD_NEK2_1 | 297 | 302 | PF00069 | 0.600 |
MOD_NEK2_1 | 379 | 384 | PF00069 | 0.571 |
MOD_PKA_1 | 439 | 445 | PF00069 | 0.658 |
MOD_PKA_2 | 213 | 219 | PF00069 | 0.437 |
MOD_PKA_2 | 380 | 386 | PF00069 | 0.484 |
MOD_Plk_1 | 194 | 200 | PF00069 | 0.497 |
MOD_Plk_1 | 202 | 208 | PF00069 | 0.441 |
MOD_Plk_4 | 152 | 158 | PF00069 | 0.604 |
MOD_Plk_4 | 213 | 219 | PF00069 | 0.475 |
MOD_Plk_4 | 267 | 273 | PF00069 | 0.517 |
MOD_Plk_4 | 431 | 437 | PF00069 | 0.650 |
MOD_ProDKin_1 | 125 | 131 | PF00069 | 0.633 |
MOD_ProDKin_1 | 141 | 147 | PF00069 | 0.725 |
MOD_ProDKin_1 | 148 | 154 | PF00069 | 0.609 |
MOD_ProDKin_1 | 156 | 162 | PF00069 | 0.433 |
MOD_ProDKin_1 | 245 | 251 | PF00069 | 0.667 |
MOD_ProDKin_1 | 26 | 32 | PF00069 | 0.484 |
MOD_ProDKin_1 | 272 | 278 | PF00069 | 0.755 |
MOD_ProDKin_1 | 281 | 287 | PF00069 | 0.644 |
MOD_ProDKin_1 | 365 | 371 | PF00069 | 0.443 |
MOD_SUMO_for_1 | 258 | 261 | PF00179 | 0.628 |
TRG_DiLeu_BaEn_4 | 239 | 245 | PF01217 | 0.634 |
TRG_DiLeu_BaLyEn_6 | 404 | 409 | PF01217 | 0.641 |
TRG_ENDOCYTIC_2 | 247 | 250 | PF00928 | 0.620 |
TRG_ENDOCYTIC_2 | 322 | 325 | PF00928 | 0.395 |
TRG_ENDOCYTIC_2 | 79 | 82 | PF00928 | 0.569 |
TRG_ER_diArg_1 | 108 | 111 | PF00400 | 0.782 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZQ4 | Leptomonas seymouri | 49% | 98% |
A0A3S5H7Z2 | Leishmania donovani | 91% | 100% |
A4HML4 | Leishmania braziliensis | 78% | 100% |
A4IB91 | Leishmania infantum | 91% | 100% |
E9AF15 | Leishmania major | 90% | 100% |