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: A4HZC3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 342 | 346 | PF00656 | 0.646 |
CLV_C14_Caspase3-7 | 399 | 403 | PF00656 | 0.733 |
CLV_C14_Caspase3-7 | 421 | 425 | PF00656 | 0.742 |
CLV_C14_Caspase3-7 | 486 | 490 | PF00656 | 0.642 |
CLV_NRD_NRD_1 | 201 | 203 | PF00675 | 0.666 |
CLV_NRD_NRD_1 | 205 | 207 | PF00675 | 0.629 |
CLV_NRD_NRD_1 | 213 | 215 | PF00675 | 0.571 |
CLV_NRD_NRD_1 | 97 | 99 | PF00675 | 0.530 |
CLV_PCSK_KEX2_1 | 201 | 203 | PF00082 | 0.666 |
CLV_PCSK_KEX2_1 | 205 | 207 | PF00082 | 0.629 |
CLV_PCSK_KEX2_1 | 213 | 215 | PF00082 | 0.571 |
CLV_PCSK_KEX2_1 | 97 | 99 | PF00082 | 0.530 |
CLV_PCSK_PC7_1 | 201 | 207 | PF00082 | 0.684 |
CLV_PCSK_SKI1_1 | 189 | 193 | PF00082 | 0.530 |
DEG_APCC_DBOX_1 | 188 | 196 | PF00400 | 0.522 |
DEG_APCC_DBOX_1 | 212 | 220 | PF00400 | 0.697 |
DEG_APCC_DBOX_1 | 62 | 70 | PF00400 | 0.530 |
DOC_CYCLIN_RxL_1 | 186 | 196 | PF00134 | 0.526 |
DOC_CYCLIN_RxL_1 | 35 | 44 | PF00134 | 0.316 |
DOC_CYCLIN_RxL_1 | 79 | 89 | PF00134 | 0.541 |
DOC_USP7_MATH_1 | 149 | 153 | PF00917 | 0.699 |
DOC_USP7_MATH_1 | 228 | 232 | PF00917 | 0.804 |
DOC_USP7_MATH_1 | 279 | 283 | PF00917 | 0.600 |
DOC_USP7_MATH_1 | 329 | 333 | PF00917 | 0.605 |
DOC_USP7_MATH_1 | 431 | 435 | PF00917 | 0.668 |
DOC_WW_Pin1_4 | 154 | 159 | PF00397 | 0.671 |
DOC_WW_Pin1_4 | 233 | 238 | PF00397 | 0.761 |
DOC_WW_Pin1_4 | 264 | 269 | PF00397 | 0.722 |
DOC_WW_Pin1_4 | 351 | 356 | PF00397 | 0.781 |
DOC_WW_Pin1_4 | 412 | 417 | PF00397 | 0.796 |
LIG_14-3-3_CanoR_1 | 125 | 133 | PF00244 | 0.595 |
LIG_14-3-3_CanoR_1 | 206 | 216 | PF00244 | 0.661 |
LIG_14-3-3_CanoR_1 | 238 | 247 | PF00244 | 0.748 |
LIG_14-3-3_CanoR_1 | 38 | 43 | PF00244 | 0.316 |
LIG_14-3-3_CanoR_1 | 411 | 418 | PF00244 | 0.710 |
LIG_14-3-3_CanoR_1 | 63 | 67 | PF00244 | 0.530 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.512 |
LIG_BIR_III_2 | 489 | 493 | PF00653 | 0.706 |
LIG_EVH1_1 | 451 | 455 | PF00568 | 0.744 |
LIG_FHA_1 | 42 | 48 | PF00498 | 0.452 |
LIG_FHA_1 | 66 | 72 | PF00498 | 0.452 |
LIG_FHA_2 | 419 | 425 | PF00498 | 0.736 |
LIG_LIR_Apic_2 | 449 | 454 | PF02991 | 0.758 |
LIG_LIR_Nem_3 | 424 | 429 | PF02991 | 0.755 |
LIG_PDZ_Class_3 | 493 | 498 | PF00595 | 0.673 |
LIG_PTB_Apo_2 | 87 | 94 | PF02174 | 0.460 |
LIG_Rb_LxCxE_1 | 157 | 174 | PF01857 | 0.586 |
LIG_SH2_NCK_1 | 326 | 330 | PF00017 | 0.705 |
LIG_SH2_STAT3 | 369 | 372 | PF00017 | 0.652 |
LIG_SH2_STAT5 | 369 | 372 | PF00017 | 0.554 |
LIG_SH3_2 | 391 | 396 | PF14604 | 0.625 |
LIG_SH3_2 | 452 | 457 | PF14604 | 0.731 |
LIG_SH3_3 | 152 | 158 | PF00018 | 0.623 |
LIG_SH3_3 | 244 | 250 | PF00018 | 0.793 |
LIG_SH3_3 | 388 | 394 | PF00018 | 0.623 |
LIG_SH3_3 | 414 | 420 | PF00018 | 0.790 |
LIG_SH3_3 | 449 | 455 | PF00018 | 0.650 |
LIG_SH3_5 | 322 | 326 | PF00018 | 0.743 |
LIG_SUMO_SIM_par_1 | 2 | 10 | PF11976 | 0.615 |
LIG_SUMO_SIM_par_1 | 38 | 44 | PF11976 | 0.530 |
LIG_SUMO_SIM_par_1 | 67 | 72 | PF11976 | 0.452 |
MOD_CDK_SPK_2 | 233 | 238 | PF00069 | 0.742 |
MOD_CK1_1 | 142 | 148 | PF00069 | 0.758 |
MOD_CK1_1 | 351 | 357 | PF00069 | 0.734 |
MOD_CK1_1 | 41 | 47 | PF00069 | 0.415 |
MOD_CK1_1 | 412 | 418 | PF00069 | 0.702 |
MOD_CK1_1 | 419 | 425 | PF00069 | 0.643 |
MOD_CK1_1 | 72 | 78 | PF00069 | 0.333 |
MOD_CK2_1 | 380 | 386 | PF00069 | 0.766 |
MOD_GlcNHglycan | 141 | 144 | PF01048 | 0.787 |
MOD_GlcNHglycan | 147 | 150 | PF01048 | 0.712 |
MOD_GlcNHglycan | 151 | 154 | PF01048 | 0.619 |
MOD_GlcNHglycan | 21 | 24 | PF01048 | 0.453 |
MOD_GlcNHglycan | 223 | 226 | PF01048 | 0.796 |
MOD_GlcNHglycan | 229 | 233 | PF01048 | 0.725 |
MOD_GlcNHglycan | 240 | 243 | PF01048 | 0.649 |
MOD_GlcNHglycan | 327 | 330 | PF01048 | 0.811 |
MOD_GlcNHglycan | 333 | 336 | PF01048 | 0.714 |
MOD_GlcNHglycan | 380 | 383 | PF01048 | 0.743 |
MOD_GlcNHglycan | 397 | 401 | PF01048 | 0.549 |
MOD_GlcNHglycan | 421 | 424 | PF01048 | 0.688 |
MOD_GlcNHglycan | 432 | 436 | PF01048 | 0.727 |
MOD_GlcNHglycan | 93 | 96 | PF01048 | 0.480 |
MOD_GSK3_1 | 120 | 127 | PF00069 | 0.486 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.684 |
MOD_GSK3_1 | 208 | 215 | PF00069 | 0.706 |
MOD_GSK3_1 | 325 | 332 | PF00069 | 0.646 |
MOD_GSK3_1 | 367 | 374 | PF00069 | 0.633 |
MOD_GSK3_1 | 380 | 387 | PF00069 | 0.599 |
MOD_GSK3_1 | 405 | 412 | PF00069 | 0.638 |
MOD_GSK3_1 | 65 | 72 | PF00069 | 0.413 |
MOD_LATS_1 | 378 | 384 | PF00433 | 0.827 |
MOD_N-GLC_1 | 77 | 82 | PF02516 | 0.512 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.658 |
MOD_NEK2_1 | 207 | 212 | PF00069 | 0.611 |
MOD_NEK2_1 | 40 | 45 | PF00069 | 0.444 |
MOD_NEK2_1 | 410 | 415 | PF00069 | 0.607 |
MOD_NEK2_1 | 69 | 74 | PF00069 | 0.431 |
MOD_NEK2_1 | 86 | 91 | PF00069 | 0.466 |
MOD_NEK2_2 | 120 | 125 | PF00069 | 0.678 |
MOD_NEK2_2 | 62 | 67 | PF00069 | 0.530 |
MOD_NEK2_2 | 77 | 82 | PF00069 | 0.342 |
MOD_PIKK_1 | 208 | 214 | PF00454 | 0.708 |
MOD_PK_1 | 380 | 386 | PF00069 | 0.753 |
MOD_PKA_2 | 124 | 130 | PF00069 | 0.554 |
MOD_PKA_2 | 193 | 199 | PF00069 | 0.555 |
MOD_PKA_2 | 212 | 218 | PF00069 | 0.511 |
MOD_PKA_2 | 221 | 227 | PF00069 | 0.608 |
MOD_PKA_2 | 301 | 307 | PF00069 | 0.726 |
MOD_PKA_2 | 410 | 416 | PF00069 | 0.658 |
MOD_PKA_2 | 62 | 68 | PF00069 | 0.530 |
MOD_Plk_1 | 178 | 184 | PF00069 | 0.566 |
MOD_Plk_1 | 329 | 335 | PF00069 | 0.644 |
MOD_Plk_1 | 77 | 83 | PF00069 | 0.410 |
MOD_Plk_4 | 1 | 7 | PF00069 | 0.650 |
MOD_Plk_4 | 359 | 365 | PF00069 | 0.695 |
MOD_ProDKin_1 | 154 | 160 | PF00069 | 0.673 |
MOD_ProDKin_1 | 233 | 239 | PF00069 | 0.761 |
MOD_ProDKin_1 | 264 | 270 | PF00069 | 0.724 |
MOD_ProDKin_1 | 351 | 357 | PF00069 | 0.780 |
MOD_ProDKin_1 | 412 | 418 | PF00069 | 0.797 |
MOD_SUMO_rev_2 | 334 | 343 | PF00179 | 0.605 |
TRG_ER_diArg_1 | 205 | 207 | PF00400 | 0.667 |
TRG_ER_diArg_1 | 96 | 98 | PF00400 | 0.530 |
TRG_Pf-PMV_PEXEL_1 | 189 | 193 | PF00026 | 0.569 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7WWT1 | Leishmania donovani | 99% | 100% |
A4HBY1 | Leishmania braziliensis | 56% | 97% |
E9AVB0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 98% |
Q4QC70 | Leishmania major | 85% | 100% |