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: 5 |
NetGPI | no | yes: 0, no: 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005929 | cilium | 4 | 6 |
GO:0042995 | cell projection | 2 | 6 |
GO:0043226 | organelle | 2 | 6 |
GO:0043227 | membrane-bounded organelle | 3 | 6 |
GO:0110165 | cellular anatomical entity | 1 | 6 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 6 |
Related structures:
AlphaFold database: E9AVB0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 240 | 244 | PF00656 | 0.661 |
CLV_C14_Caspase3-7 | 342 | 346 | PF00656 | 0.664 |
CLV_C14_Caspase3-7 | 399 | 403 | PF00656 | 0.714 |
CLV_C14_Caspase3-7 | 421 | 425 | PF00656 | 0.746 |
CLV_C14_Caspase3-7 | 478 | 482 | PF00656 | 0.631 |
CLV_NRD_NRD_1 | 201 | 203 | PF00675 | 0.637 |
CLV_NRD_NRD_1 | 205 | 207 | PF00675 | 0.599 |
CLV_NRD_NRD_1 | 214 | 216 | PF00675 | 0.545 |
CLV_NRD_NRD_1 | 379 | 381 | PF00675 | 0.718 |
CLV_NRD_NRD_1 | 97 | 99 | PF00675 | 0.580 |
CLV_PCSK_KEX2_1 | 201 | 203 | PF00082 | 0.637 |
CLV_PCSK_KEX2_1 | 205 | 207 | PF00082 | 0.599 |
CLV_PCSK_KEX2_1 | 213 | 215 | PF00082 | 0.564 |
CLV_PCSK_KEX2_1 | 379 | 381 | PF00082 | 0.718 |
CLV_PCSK_KEX2_1 | 97 | 99 | PF00082 | 0.580 |
CLV_PCSK_PC7_1 | 201 | 207 | PF00082 | 0.654 |
CLV_PCSK_SKI1_1 | 464 | 468 | PF00082 | 0.524 |
DEG_APCC_DBOX_1 | 212 | 220 | PF00400 | 0.678 |
DEG_APCC_DBOX_1 | 62 | 70 | PF00400 | 0.587 |
DOC_CKS1_1 | 33 | 38 | PF01111 | 0.326 |
DOC_USP7_MATH_1 | 149 | 153 | PF00917 | 0.670 |
DOC_USP7_MATH_1 | 221 | 225 | PF00917 | 0.649 |
DOC_USP7_MATH_1 | 237 | 241 | PF00917 | 0.647 |
DOC_USP7_MATH_1 | 391 | 395 | PF00917 | 0.708 |
DOC_USP7_MATH_1 | 420 | 424 | PF00917 | 0.695 |
DOC_USP7_MATH_1 | 431 | 435 | PF00917 | 0.695 |
DOC_WW_Pin1_4 | 154 | 159 | PF00397 | 0.647 |
DOC_WW_Pin1_4 | 207 | 212 | PF00397 | 0.414 |
DOC_WW_Pin1_4 | 233 | 238 | PF00397 | 0.755 |
DOC_WW_Pin1_4 | 251 | 256 | PF00397 | 0.549 |
DOC_WW_Pin1_4 | 264 | 269 | PF00397 | 0.714 |
DOC_WW_Pin1_4 | 32 | 37 | PF00397 | 0.330 |
DOC_WW_Pin1_4 | 351 | 356 | PF00397 | 0.783 |
DOC_WW_Pin1_4 | 411 | 416 | PF00397 | 0.779 |
LIG_14-3-3_CanoR_1 | 238 | 247 | PF00244 | 0.762 |
LIG_14-3-3_CanoR_1 | 302 | 307 | PF00244 | 0.505 |
LIG_14-3-3_CanoR_1 | 404 | 412 | PF00244 | 0.621 |
LIG_14-3-3_CanoR_1 | 63 | 67 | PF00244 | 0.597 |
LIG_Actin_WH2_2 | 381 | 398 | PF00022 | 0.634 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.487 |
LIG_BIR_III_2 | 481 | 485 | PF00653 | 0.691 |
LIG_EVH1_1 | 446 | 450 | PF00568 | 0.726 |
LIG_FHA_1 | 194 | 200 | PF00498 | 0.330 |
LIG_FHA_1 | 42 | 48 | PF00498 | 0.513 |
LIG_FHA_1 | 66 | 72 | PF00498 | 0.499 |
LIG_FHA_2 | 419 | 425 | PF00498 | 0.741 |
LIG_LIR_Apic_2 | 444 | 449 | PF02991 | 0.737 |
LIG_LIR_Gen_1 | 91 | 101 | PF02991 | 0.370 |
LIG_LIR_Nem_3 | 174 | 178 | PF02991 | 0.544 |
LIG_LIR_Nem_3 | 91 | 96 | PF02991 | 0.369 |
LIG_PCNA_yPIPBox_3 | 75 | 85 | PF02747 | 0.283 |
LIG_RPA_C_Fungi | 196 | 208 | PF08784 | 0.406 |
LIG_SH2_PTP2 | 175 | 178 | PF00017 | 0.542 |
LIG_SH2_STAT3 | 369 | 372 | PF00017 | 0.661 |
LIG_SH2_STAT5 | 145 | 148 | PF00017 | 0.486 |
LIG_SH2_STAT5 | 175 | 178 | PF00017 | 0.542 |
LIG_SH2_STAT5 | 326 | 329 | PF00017 | 0.619 |
LIG_SH2_STAT5 | 369 | 372 | PF00017 | 0.564 |
LIG_SH2_STAT5 | 429 | 432 | PF00017 | 0.645 |
LIG_SH3_2 | 447 | 452 | PF14604 | 0.734 |
LIG_SH3_3 | 244 | 250 | PF00018 | 0.812 |
LIG_SH3_3 | 356 | 362 | PF00018 | 0.545 |
LIG_SH3_3 | 409 | 415 | PF00018 | 0.730 |
LIG_SH3_3 | 444 | 450 | PF00018 | 0.630 |
LIG_SH3_5 | 322 | 326 | PF00018 | 0.740 |
LIG_SUMO_SIM_par_1 | 2 | 10 | PF11976 | 0.596 |
LIG_SUMO_SIM_par_1 | 38 | 44 | PF11976 | 0.592 |
LIG_SUMO_SIM_par_1 | 67 | 72 | PF11976 | 0.502 |
LIG_TYR_ITIM | 173 | 178 | PF00017 | 0.546 |
LIG_UBA3_1 | 457 | 464 | PF00899 | 0.519 |
MOD_CDC14_SPxK_1 | 210 | 213 | PF00782 | 0.433 |
MOD_CDK_SPK_2 | 233 | 238 | PF00069 | 0.736 |
MOD_CDK_SPxK_1 | 207 | 213 | PF00069 | 0.422 |
MOD_CDK_SPxxK_3 | 207 | 214 | PF00069 | 0.428 |
MOD_CK1_1 | 14 | 20 | PF00069 | 0.316 |
MOD_CK1_1 | 22 | 28 | PF00069 | 0.284 |
MOD_CK1_1 | 351 | 357 | PF00069 | 0.738 |
MOD_CK1_1 | 41 | 47 | PF00069 | 0.476 |
MOD_CK1_1 | 419 | 425 | PF00069 | 0.649 |
MOD_CK1_1 | 91 | 97 | PF00069 | 0.499 |
MOD_CK2_1 | 391 | 397 | PF00069 | 0.714 |
MOD_CK2_1 | 431 | 437 | PF00069 | 0.538 |
MOD_GlcNHglycan | 147 | 150 | PF01048 | 0.682 |
MOD_GlcNHglycan | 151 | 154 | PF01048 | 0.594 |
MOD_GlcNHglycan | 21 | 24 | PF01048 | 0.428 |
MOD_GlcNHglycan | 223 | 226 | PF01048 | 0.747 |
MOD_GlcNHglycan | 240 | 243 | PF01048 | 0.658 |
MOD_GlcNHglycan | 327 | 330 | PF01048 | 0.806 |
MOD_GlcNHglycan | 333 | 336 | PF01048 | 0.724 |
MOD_GlcNHglycan | 345 | 349 | PF01048 | 0.568 |
MOD_GlcNHglycan | 380 | 383 | PF01048 | 0.748 |
MOD_GlcNHglycan | 397 | 401 | PF01048 | 0.536 |
MOD_GlcNHglycan | 433 | 436 | PF01048 | 0.740 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.488 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.658 |
MOD_GSK3_1 | 233 | 240 | PF00069 | 0.623 |
MOD_GSK3_1 | 325 | 332 | PF00069 | 0.643 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.645 |
MOD_GSK3_1 | 367 | 374 | PF00069 | 0.645 |
MOD_GSK3_1 | 380 | 387 | PF00069 | 0.599 |
MOD_GSK3_1 | 416 | 423 | PF00069 | 0.777 |
MOD_GSK3_1 | 427 | 434 | PF00069 | 0.535 |
MOD_GSK3_1 | 65 | 72 | PF00069 | 0.462 |
MOD_LATS_1 | 378 | 384 | PF00433 | 0.834 |
MOD_N-GLC_1 | 391 | 396 | PF02516 | 0.677 |
MOD_N-GLC_1 | 77 | 82 | PF02516 | 0.497 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.633 |
MOD_NEK2_1 | 344 | 349 | PF00069 | 0.551 |
MOD_NEK2_1 | 86 | 91 | PF00069 | 0.452 |
MOD_NEK2_2 | 120 | 125 | PF00069 | 0.633 |
MOD_NEK2_2 | 391 | 396 | PF00069 | 0.638 |
MOD_NEK2_2 | 62 | 67 | PF00069 | 0.590 |
MOD_PK_1 | 302 | 308 | PF00069 | 0.504 |
MOD_PK_1 | 380 | 386 | PF00069 | 0.755 |
MOD_PKA_1 | 214 | 220 | PF00069 | 0.465 |
MOD_PKA_2 | 193 | 199 | PF00069 | 0.544 |
MOD_PKA_2 | 214 | 220 | PF00069 | 0.724 |
MOD_PKA_2 | 221 | 227 | PF00069 | 0.561 |
MOD_PKA_2 | 237 | 243 | PF00069 | 0.549 |
MOD_PKA_2 | 301 | 307 | PF00069 | 0.718 |
MOD_PKA_2 | 378 | 384 | PF00069 | 0.718 |
MOD_PKA_2 | 62 | 68 | PF00069 | 0.590 |
MOD_Plk_1 | 14 | 20 | PF00069 | 0.393 |
MOD_Plk_1 | 178 | 184 | PF00069 | 0.535 |
MOD_Plk_1 | 329 | 335 | PF00069 | 0.649 |
MOD_Plk_1 | 391 | 397 | PF00069 | 0.637 |
MOD_Plk_1 | 77 | 83 | PF00069 | 0.394 |
MOD_Plk_4 | 1 | 7 | PF00069 | 0.627 |
MOD_Plk_4 | 14 | 20 | PF00069 | 0.392 |
MOD_Plk_4 | 424 | 430 | PF00069 | 0.544 |
MOD_ProDKin_1 | 154 | 160 | PF00069 | 0.649 |
MOD_ProDKin_1 | 207 | 213 | PF00069 | 0.422 |
MOD_ProDKin_1 | 233 | 239 | PF00069 | 0.756 |
MOD_ProDKin_1 | 251 | 257 | PF00069 | 0.553 |
MOD_ProDKin_1 | 264 | 270 | PF00069 | 0.716 |
MOD_ProDKin_1 | 32 | 38 | PF00069 | 0.327 |
MOD_ProDKin_1 | 351 | 357 | PF00069 | 0.784 |
MOD_ProDKin_1 | 411 | 417 | PF00069 | 0.779 |
TRG_DiLeu_BaLyEn_6 | 359 | 364 | PF01217 | 0.517 |
TRG_ENDOCYTIC_2 | 175 | 178 | PF00928 | 0.542 |
TRG_ER_diArg_1 | 191 | 194 | PF00400 | 0.423 |
TRG_ER_diArg_1 | 205 | 208 | PF00400 | 0.647 |
TRG_ER_diArg_1 | 213 | 215 | PF00400 | 0.630 |
TRG_ER_diArg_1 | 96 | 98 | PF00400 | 0.579 |
TRG_Pf-PMV_PEXEL_1 | 189 | 193 | PF00026 | 0.550 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7WWT1 | Leishmania donovani | 78% | 98% |
A4HBY1 | Leishmania braziliensis | 53% | 99% |
A4HZC3 | Leishmania infantum | 78% | 98% |
Q4QC70 | Leishmania major | 77% | 100% |