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:0035869 | ciliary transition zone | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HS94
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 315 | 319 | PF00656 | 0.730 |
CLV_C14_Caspase3-7 | 380 | 384 | PF00656 | 0.553 |
CLV_NRD_NRD_1 | 176 | 178 | PF00675 | 0.726 |
CLV_NRD_NRD_1 | 27 | 29 | PF00675 | 0.709 |
CLV_NRD_NRD_1 | 438 | 440 | PF00675 | 0.740 |
CLV_NRD_NRD_1 | 486 | 488 | PF00675 | 0.675 |
CLV_NRD_NRD_1 | 63 | 65 | PF00675 | 0.780 |
CLV_PCSK_FUR_1 | 21 | 25 | PF00082 | 0.842 |
CLV_PCSK_KEX2_1 | 176 | 178 | PF00082 | 0.728 |
CLV_PCSK_KEX2_1 | 23 | 25 | PF00082 | 0.839 |
CLV_PCSK_KEX2_1 | 27 | 29 | PF00082 | 0.774 |
CLV_PCSK_KEX2_1 | 438 | 440 | PF00082 | 0.740 |
CLV_PCSK_KEX2_1 | 486 | 488 | PF00082 | 0.675 |
CLV_PCSK_KEX2_1 | 87 | 89 | PF00082 | 0.840 |
CLV_PCSK_PC1ET2_1 | 23 | 25 | PF00082 | 0.839 |
CLV_PCSK_PC1ET2_1 | 87 | 89 | PF00082 | 0.782 |
CLV_PCSK_SKI1_1 | 176 | 180 | PF00082 | 0.731 |
CLV_PCSK_SKI1_1 | 34 | 38 | PF00082 | 0.787 |
CLV_PCSK_SKI1_1 | 358 | 362 | PF00082 | 0.673 |
DEG_SCF_TRCP1_1 | 383 | 389 | PF00400 | 0.682 |
DEG_SPOP_SBC_1 | 167 | 171 | PF00917 | 0.702 |
DEG_SPOP_SBC_1 | 195 | 199 | PF00917 | 0.838 |
DEG_SPOP_SBC_1 | 54 | 58 | PF00917 | 0.831 |
DOC_CYCLIN_RxL_1 | 173 | 181 | PF00134 | 0.726 |
DOC_MAPK_DCC_7 | 253 | 261 | PF00069 | 0.713 |
DOC_MAPK_DCC_7 | 358 | 368 | PF00069 | 0.654 |
DOC_MAPK_MEF2A_6 | 253 | 261 | PF00069 | 0.713 |
DOC_MAPK_MEF2A_6 | 354 | 363 | PF00069 | 0.695 |
DOC_PP2B_LxvP_1 | 120 | 123 | PF13499 | 0.781 |
DOC_PP2B_PxIxI_1 | 256 | 262 | PF00149 | 0.702 |
DOC_USP7_MATH_1 | 196 | 200 | PF00917 | 0.762 |
DOC_USP7_MATH_1 | 209 | 213 | PF00917 | 0.620 |
DOC_USP7_MATH_1 | 245 | 249 | PF00917 | 0.523 |
DOC_USP7_MATH_1 | 292 | 296 | PF00917 | 0.556 |
DOC_USP7_MATH_1 | 455 | 459 | PF00917 | 0.485 |
DOC_USP7_MATH_1 | 54 | 58 | PF00917 | 0.829 |
DOC_USP7_MATH_1 | 63 | 67 | PF00917 | 0.732 |
DOC_WW_Pin1_4 | 113 | 118 | PF00397 | 0.618 |
DOC_WW_Pin1_4 | 121 | 126 | PF00397 | 0.674 |
DOC_WW_Pin1_4 | 152 | 157 | PF00397 | 0.738 |
DOC_WW_Pin1_4 | 2 | 7 | PF00397 | 0.757 |
DOC_WW_Pin1_4 | 251 | 256 | PF00397 | 0.620 |
DOC_WW_Pin1_4 | 264 | 269 | PF00397 | 0.672 |
DOC_WW_Pin1_4 | 36 | 41 | PF00397 | 0.625 |
DOC_WW_Pin1_4 | 386 | 391 | PF00397 | 0.689 |
DOC_WW_Pin1_4 | 59 | 64 | PF00397 | 0.777 |
DOC_WW_Pin1_4 | 98 | 103 | PF00397 | 0.823 |
LIG_14-3-3_CanoR_1 | 138 | 143 | PF00244 | 0.739 |
LIG_14-3-3_CanoR_1 | 160 | 164 | PF00244 | 0.791 |
LIG_14-3-3_CanoR_1 | 166 | 174 | PF00244 | 0.753 |
LIG_14-3-3_CanoR_1 | 21 | 27 | PF00244 | 0.765 |
LIG_14-3-3_CanoR_1 | 34 | 42 | PF00244 | 0.597 |
LIG_14-3-3_CanoR_1 | 347 | 356 | PF00244 | 0.729 |
LIG_14-3-3_CanoR_1 | 392 | 397 | PF00244 | 0.486 |
LIG_14-3-3_CanoR_1 | 418 | 425 | PF00244 | 0.619 |
LIG_14-3-3_CanoR_1 | 64 | 71 | PF00244 | 0.761 |
LIG_Actin_WH2_2 | 417 | 434 | PF00022 | 0.689 |
LIG_APCC_ABBA_1 | 417 | 422 | PF00400 | 0.687 |
LIG_BRCT_BRCA1_1 | 154 | 158 | PF00533 | 0.629 |
LIG_FHA_1 | 122 | 128 | PF00498 | 0.852 |
LIG_FHA_1 | 169 | 175 | PF00498 | 0.753 |
LIG_FHA_1 | 200 | 206 | PF00498 | 0.635 |
LIG_FHA_1 | 256 | 262 | PF00498 | 0.585 |
LIG_FHA_1 | 37 | 43 | PF00498 | 0.632 |
LIG_FHA_1 | 99 | 105 | PF00498 | 0.670 |
LIG_FHA_2 | 457 | 463 | PF00498 | 0.642 |
LIG_LIR_Apic_2 | 263 | 268 | PF02991 | 0.735 |
LIG_LIR_Apic_2 | 470 | 476 | PF02991 | 0.713 |
LIG_PTAP_UEV_1 | 210 | 215 | PF05743 | 0.652 |
LIG_SH2_CRK | 265 | 269 | PF00017 | 0.753 |
LIG_SH2_CRK | 473 | 477 | PF00017 | 0.656 |
LIG_SH2_STAT5 | 29 | 32 | PF00017 | 0.691 |
LIG_SH2_STAT5 | 401 | 404 | PF00017 | 0.672 |
LIG_SH3_3 | 120 | 126 | PF00018 | 0.839 |
LIG_SH3_3 | 161 | 167 | PF00018 | 0.780 |
LIG_SH3_3 | 201 | 207 | PF00018 | 0.707 |
LIG_SH3_3 | 208 | 214 | PF00018 | 0.622 |
LIG_SH3_3 | 384 | 390 | PF00018 | 0.689 |
LIG_SH3_3 | 39 | 45 | PF00018 | 0.821 |
LIG_SH3_3 | 413 | 419 | PF00018 | 0.612 |
LIG_SH3_3 | 68 | 74 | PF00018 | 0.825 |
LIG_TRAF2_1 | 340 | 343 | PF00917 | 0.689 |
LIG_TRAF2_1 | 459 | 462 | PF00917 | 0.523 |
LIG_TRFH_1 | 238 | 242 | PF08558 | 0.806 |
LIG_TRFH_1 | 29 | 33 | PF08558 | 0.647 |
MOD_CDC14_SPxK_1 | 389 | 392 | PF00782 | 0.463 |
MOD_CDC14_SPxK_1 | 62 | 65 | PF00782 | 0.780 |
MOD_CDK_SPK_2 | 59 | 64 | PF00069 | 0.777 |
MOD_CDK_SPxK_1 | 386 | 392 | PF00069 | 0.477 |
MOD_CDK_SPxK_1 | 59 | 65 | PF00069 | 0.778 |
MOD_CK1_1 | 141 | 147 | PF00069 | 0.816 |
MOD_CK1_1 | 152 | 158 | PF00069 | 0.702 |
MOD_CK1_1 | 181 | 187 | PF00069 | 0.782 |
MOD_CK1_1 | 197 | 203 | PF00069 | 0.582 |
MOD_CK1_1 | 5 | 11 | PF00069 | 0.804 |
MOD_CK1_1 | 98 | 104 | PF00069 | 0.763 |
MOD_CK2_1 | 337 | 343 | PF00069 | 0.736 |
MOD_CK2_1 | 392 | 398 | PF00069 | 0.632 |
MOD_CK2_1 | 456 | 462 | PF00069 | 0.529 |
MOD_GlcNHglycan | 104 | 107 | PF01048 | 0.831 |
MOD_GlcNHglycan | 134 | 137 | PF01048 | 0.836 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.727 |
MOD_GlcNHglycan | 190 | 193 | PF01048 | 0.741 |
MOD_GlcNHglycan | 211 | 214 | PF01048 | 0.658 |
MOD_GlcNHglycan | 216 | 219 | PF01048 | 0.639 |
MOD_GlcNHglycan | 247 | 250 | PF01048 | 0.531 |
MOD_GlcNHglycan | 298 | 301 | PF01048 | 0.686 |
MOD_GlcNHglycan | 383 | 386 | PF01048 | 0.671 |
MOD_GlcNHglycan | 394 | 397 | PF01048 | 0.599 |
MOD_GlcNHglycan | 57 | 60 | PF01048 | 0.696 |
MOD_GlcNHglycan | 65 | 68 | PF01048 | 0.716 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.700 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.718 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.748 |
MOD_GSK3_1 | 236 | 243 | PF00069 | 0.791 |
MOD_GSK3_1 | 251 | 258 | PF00069 | 0.498 |
MOD_GSK3_1 | 292 | 299 | PF00069 | 0.722 |
MOD_GSK3_1 | 318 | 325 | PF00069 | 0.760 |
MOD_GSK3_1 | 377 | 384 | PF00069 | 0.640 |
MOD_GSK3_1 | 4 | 11 | PF00069 | 0.745 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.827 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.732 |
MOD_NEK2_1 | 178 | 183 | PF00069 | 0.727 |
MOD_NEK2_2 | 236 | 241 | PF00069 | 0.777 |
MOD_PKA_1 | 87 | 93 | PF00069 | 0.787 |
MOD_PKA_2 | 159 | 165 | PF00069 | 0.738 |
MOD_PKA_2 | 181 | 187 | PF00069 | 0.747 |
MOD_PKA_2 | 188 | 194 | PF00069 | 0.670 |
MOD_PKA_2 | 240 | 246 | PF00069 | 0.743 |
MOD_PKA_2 | 391 | 397 | PF00069 | 0.477 |
MOD_PKA_2 | 63 | 69 | PF00069 | 0.760 |
MOD_PKA_2 | 87 | 93 | PF00069 | 0.787 |
MOD_Plk_2-3 | 318 | 324 | PF00069 | 0.760 |
MOD_ProDKin_1 | 113 | 119 | PF00069 | 0.620 |
MOD_ProDKin_1 | 121 | 127 | PF00069 | 0.678 |
MOD_ProDKin_1 | 152 | 158 | PF00069 | 0.739 |
MOD_ProDKin_1 | 2 | 8 | PF00069 | 0.757 |
MOD_ProDKin_1 | 251 | 257 | PF00069 | 0.618 |
MOD_ProDKin_1 | 264 | 270 | PF00069 | 0.665 |
MOD_ProDKin_1 | 36 | 42 | PF00069 | 0.628 |
MOD_ProDKin_1 | 386 | 392 | PF00069 | 0.691 |
MOD_ProDKin_1 | 59 | 65 | PF00069 | 0.778 |
MOD_ProDKin_1 | 98 | 104 | PF00069 | 0.825 |
TRG_DiLeu_BaLyEn_6 | 174 | 179 | PF01217 | 0.634 |
TRG_ENDOCYTIC_2 | 329 | 332 | PF00928 | 0.764 |
TRG_ER_diArg_1 | 176 | 178 | PF00400 | 0.763 |
TRG_ER_diArg_1 | 26 | 28 | PF00400 | 0.717 |
TRG_ER_diArg_1 | 274 | 277 | PF00400 | 0.658 |
TRG_ER_diArg_1 | 438 | 440 | PF00400 | 0.740 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S5H5D8 | Leishmania donovani | 100% | 93% |
A4H411 | Leishmania braziliensis | 65% | 100% |
E9AK78 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 98% |
Q9U1D2 | Leishmania major | 84% | 100% |