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: E9B1T2
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 7 |
GO:0005488 | binding | 1 | 7 |
GO:0097159 | organic cyclic compound binding | 2 | 7 |
GO:1901363 | heterocyclic compound binding | 2 | 7 |
GO:0003677 | DNA binding | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 364 | 368 | PF00656 | 0.597 |
CLV_C14_Caspase3-7 | 474 | 478 | PF00656 | 0.498 |
CLV_NRD_NRD_1 | 237 | 239 | PF00675 | 0.520 |
CLV_PCSK_KEX2_1 | 340 | 342 | PF00082 | 0.433 |
CLV_PCSK_PC1ET2_1 | 340 | 342 | PF00082 | 0.433 |
CLV_PCSK_SKI1_1 | 319 | 323 | PF00082 | 0.464 |
CLV_PCSK_SKI1_1 | 395 | 399 | PF00082 | 0.357 |
DEG_COP1_1 | 269 | 280 | PF00400 | 0.618 |
DEG_COP1_1 | 302 | 312 | PF00400 | 0.453 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.574 |
DEG_SPOP_SBC_1 | 162 | 166 | PF00917 | 0.693 |
DEG_SPOP_SBC_1 | 167 | 171 | PF00917 | 0.638 |
DEG_SPOP_SBC_1 | 250 | 254 | PF00917 | 0.611 |
DOC_MAPK_DCC_7 | 394 | 402 | PF00069 | 0.350 |
DOC_MAPK_gen_1 | 238 | 245 | PF00069 | 0.563 |
DOC_MAPK_gen_1 | 394 | 402 | PF00069 | 0.465 |
DOC_PP1_RVXF_1 | 423 | 429 | PF00149 | 0.477 |
DOC_PP2B_LxvP_1 | 281 | 284 | PF13499 | 0.647 |
DOC_PP2B_LxvP_1 | 312 | 315 | PF13499 | 0.590 |
DOC_PP2B_LxvP_1 | 78 | 81 | PF13499 | 0.468 |
DOC_PP4_FxxP_1 | 307 | 310 | PF00568 | 0.736 |
DOC_PP4_MxPP_1 | 259 | 262 | PF00568 | 0.555 |
DOC_PP4_MxPP_1 | 450 | 453 | PF00568 | 0.416 |
DOC_SPAK_OSR1_1 | 427 | 431 | PF12202 | 0.503 |
DOC_USP7_MATH_1 | 250 | 254 | PF00917 | 0.585 |
DOC_USP7_MATH_1 | 264 | 268 | PF00917 | 0.677 |
DOC_USP7_MATH_1 | 284 | 288 | PF00917 | 0.589 |
DOC_USP7_MATH_1 | 373 | 377 | PF00917 | 0.579 |
DOC_USP7_MATH_1 | 57 | 61 | PF00917 | 0.508 |
DOC_USP7_UBL2_3 | 391 | 395 | PF12436 | 0.401 |
DOC_WW_Pin1_4 | 109 | 114 | PF00397 | 0.770 |
DOC_WW_Pin1_4 | 137 | 142 | PF00397 | 0.762 |
DOC_WW_Pin1_4 | 191 | 196 | PF00397 | 0.654 |
DOC_WW_Pin1_4 | 214 | 219 | PF00397 | 0.542 |
DOC_WW_Pin1_4 | 232 | 237 | PF00397 | 0.495 |
DOC_WW_Pin1_4 | 302 | 307 | PF00397 | 0.560 |
DOC_WW_Pin1_4 | 369 | 374 | PF00397 | 0.692 |
DOC_WW_Pin1_4 | 395 | 400 | PF00397 | 0.494 |
LIG_14-3-3_CanoR_1 | 319 | 325 | PF00244 | 0.622 |
LIG_14-3-3_CanoR_1 | 76 | 81 | PF00244 | 0.573 |
LIG_BRCT_BRCA1_1 | 303 | 307 | PF00533 | 0.620 |
LIG_EVH1_1 | 314 | 318 | PF00568 | 0.583 |
LIG_FHA_1 | 162 | 168 | PF00498 | 0.511 |
LIG_FHA_1 | 229 | 235 | PF00498 | 0.539 |
LIG_FHA_1 | 309 | 315 | PF00498 | 0.488 |
LIG_FHA_1 | 352 | 358 | PF00498 | 0.430 |
LIG_FHA_1 | 417 | 423 | PF00498 | 0.499 |
LIG_FHA_2 | 242 | 248 | PF00498 | 0.587 |
LIG_FHA_2 | 384 | 390 | PF00498 | 0.606 |
LIG_LIR_Apic_2 | 254 | 260 | PF02991 | 0.646 |
LIG_LIR_Apic_2 | 304 | 310 | PF02991 | 0.673 |
LIG_LIR_Apic_2 | 51 | 57 | PF02991 | 0.536 |
LIG_LIR_Nem_3 | 333 | 338 | PF02991 | 0.393 |
LIG_LIR_Nem_3 | 415 | 420 | PF02991 | 0.579 |
LIG_PCNA_PIPBox_1 | 328 | 337 | PF02747 | 0.366 |
LIG_PCNA_yPIPBox_3 | 322 | 335 | PF02747 | 0.515 |
LIG_SH2_CRK | 257 | 261 | PF00017 | 0.631 |
LIG_SH2_CRK | 54 | 58 | PF00017 | 0.585 |
LIG_SH2_CRK | 6 | 10 | PF00017 | 0.572 |
LIG_SH2_GRB2like | 6 | 9 | PF00017 | 0.600 |
LIG_SH2_NCK_1 | 257 | 261 | PF00017 | 0.631 |
LIG_SH2_STAP1 | 505 | 509 | PF00017 | 0.481 |
LIG_SH2_STAP1 | 522 | 526 | PF00017 | 0.530 |
LIG_SH2_STAT5 | 280 | 283 | PF00017 | 0.652 |
LIG_SH2_STAT5 | 54 | 57 | PF00017 | 0.446 |
LIG_SH2_STAT5 | 69 | 72 | PF00017 | 0.614 |
LIG_SH3_1 | 257 | 263 | PF00018 | 0.621 |
LIG_SH3_2 | 317 | 322 | PF14604 | 0.637 |
LIG_SH3_3 | 192 | 198 | PF00018 | 0.728 |
LIG_SH3_3 | 201 | 207 | PF00018 | 0.591 |
LIG_SH3_3 | 215 | 221 | PF00018 | 0.578 |
LIG_SH3_3 | 22 | 28 | PF00018 | 0.673 |
LIG_SH3_3 | 257 | 263 | PF00018 | 0.666 |
LIG_SH3_3 | 307 | 313 | PF00018 | 0.748 |
LIG_SH3_3 | 314 | 320 | PF00018 | 0.615 |
LIG_SH3_3 | 477 | 483 | PF00018 | 0.573 |
LIG_TRAF2_1 | 387 | 390 | PF00917 | 0.463 |
LIG_WRC_WIRS_1 | 286 | 291 | PF05994 | 0.592 |
LIG_WW_3 | 316 | 320 | PF00397 | 0.574 |
MOD_CDK_SPxK_1 | 232 | 238 | PF00069 | 0.501 |
MOD_CDK_SPxxK_3 | 232 | 239 | PF00069 | 0.508 |
MOD_CK1_1 | 100 | 106 | PF00069 | 0.691 |
MOD_CK1_1 | 154 | 160 | PF00069 | 0.595 |
MOD_CK1_1 | 163 | 169 | PF00069 | 0.669 |
MOD_CK1_1 | 228 | 234 | PF00069 | 0.472 |
MOD_CK1_1 | 246 | 252 | PF00069 | 0.618 |
MOD_CK1_1 | 253 | 259 | PF00069 | 0.649 |
MOD_CK1_1 | 267 | 273 | PF00069 | 0.591 |
MOD_CK1_1 | 276 | 282 | PF00069 | 0.590 |
MOD_CK1_1 | 302 | 308 | PF00069 | 0.663 |
MOD_CK1_1 | 33 | 39 | PF00069 | 0.602 |
MOD_CK1_1 | 459 | 465 | PF00069 | 0.611 |
MOD_CK1_1 | 60 | 66 | PF00069 | 0.558 |
MOD_CK2_1 | 149 | 155 | PF00069 | 0.683 |
MOD_CK2_1 | 383 | 389 | PF00069 | 0.562 |
MOD_CK2_1 | 493 | 499 | PF00069 | 0.481 |
MOD_GlcNHglycan | 102 | 105 | PF01048 | 0.617 |
MOD_GlcNHglycan | 173 | 176 | PF01048 | 0.805 |
MOD_GlcNHglycan | 247 | 251 | PF01048 | 0.652 |
MOD_GlcNHglycan | 270 | 273 | PF01048 | 0.752 |
MOD_GlcNHglycan | 301 | 304 | PF01048 | 0.698 |
MOD_GlcNHglycan | 367 | 370 | PF01048 | 0.615 |
MOD_GlcNHglycan | 459 | 462 | PF01048 | 0.570 |
MOD_GlcNHglycan | 93 | 96 | PF01048 | 0.619 |
MOD_GSK3_1 | 137 | 144 | PF00069 | 0.689 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.546 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.580 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.715 |
MOD_GSK3_1 | 180 | 187 | PF00069 | 0.574 |
MOD_GSK3_1 | 205 | 212 | PF00069 | 0.794 |
MOD_GSK3_1 | 228 | 235 | PF00069 | 0.601 |
MOD_GSK3_1 | 241 | 248 | PF00069 | 0.628 |
MOD_GSK3_1 | 249 | 256 | PF00069 | 0.607 |
MOD_GSK3_1 | 264 | 271 | PF00069 | 0.690 |
MOD_GSK3_1 | 272 | 279 | PF00069 | 0.623 |
MOD_GSK3_1 | 295 | 302 | PF00069 | 0.634 |
MOD_GSK3_1 | 351 | 358 | PF00069 | 0.506 |
MOD_GSK3_1 | 361 | 368 | PF00069 | 0.514 |
MOD_GSK3_1 | 369 | 376 | PF00069 | 0.672 |
MOD_GSK3_1 | 4 | 11 | PF00069 | 0.710 |
MOD_GSK3_1 | 455 | 462 | PF00069 | 0.534 |
MOD_GSK3_1 | 65 | 72 | PF00069 | 0.774 |
MOD_N-GLC_1 | 184 | 189 | PF02516 | 0.651 |
MOD_N-GLC_1 | 377 | 382 | PF02516 | 0.614 |
MOD_NEK2_1 | 160 | 165 | PF00069 | 0.737 |
MOD_NEK2_1 | 20 | 25 | PF00069 | 0.678 |
MOD_NEK2_1 | 200 | 205 | PF00069 | 0.543 |
MOD_NEK2_1 | 225 | 230 | PF00069 | 0.504 |
MOD_NEK2_1 | 297 | 302 | PF00069 | 0.645 |
MOD_NEK2_1 | 30 | 35 | PF00069 | 0.565 |
MOD_NEK2_1 | 351 | 356 | PF00069 | 0.423 |
MOD_NEK2_1 | 457 | 462 | PF00069 | 0.606 |
MOD_NEK2_2 | 493 | 498 | PF00069 | 0.477 |
MOD_PIKK_1 | 20 | 26 | PF00454 | 0.511 |
MOD_PIKK_1 | 264 | 270 | PF00454 | 0.693 |
MOD_PIKK_1 | 33 | 39 | PF00454 | 0.602 |
MOD_PK_1 | 76 | 82 | PF00069 | 0.475 |
MOD_Plk_1 | 60 | 66 | PF00069 | 0.620 |
MOD_Plk_2-3 | 241 | 247 | PF00069 | 0.608 |
MOD_Plk_2-3 | 486 | 492 | PF00069 | 0.493 |
MOD_Plk_4 | 276 | 282 | PF00069 | 0.654 |
MOD_Plk_4 | 355 | 361 | PF00069 | 0.405 |
MOD_Plk_4 | 65 | 71 | PF00069 | 0.608 |
MOD_ProDKin_1 | 109 | 115 | PF00069 | 0.771 |
MOD_ProDKin_1 | 137 | 143 | PF00069 | 0.761 |
MOD_ProDKin_1 | 191 | 197 | PF00069 | 0.653 |
MOD_ProDKin_1 | 214 | 220 | PF00069 | 0.537 |
MOD_ProDKin_1 | 232 | 238 | PF00069 | 0.501 |
MOD_ProDKin_1 | 302 | 308 | PF00069 | 0.564 |
MOD_ProDKin_1 | 369 | 375 | PF00069 | 0.690 |
MOD_ProDKin_1 | 395 | 401 | PF00069 | 0.498 |
MOD_SUMO_for_1 | 58 | 61 | PF00179 | 0.576 |
MOD_SUMO_rev_2 | 511 | 517 | PF00179 | 0.450 |
TRG_DiLeu_BaLyEn_6 | 513 | 518 | PF01217 | 0.534 |
TRG_ENDOCYTIC_2 | 335 | 338 | PF00928 | 0.427 |
TRG_ER_diArg_1 | 425 | 428 | PF00400 | 0.477 |
TRG_Pf-PMV_PEXEL_1 | 515 | 519 | PF00026 | 0.452 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P654 | Leptomonas seymouri | 40% | 96% |
A0A3S7X4H1 | Leishmania donovani | 84% | 99% |
A4HJB7 | Leishmania braziliensis | 62% | 99% |
A4I6R0 | Leishmania infantum | 84% | 99% |
Q4Q6C9 | Leishmania major | 83% | 100% |