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: A4H411
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 321 | 325 | PF00656 | 0.598 |
CLV_C14_Caspase3-7 | 386 | 390 | PF00656 | 0.502 |
CLV_C14_Caspase3-7 | 45 | 49 | PF00656 | 0.618 |
CLV_NRD_NRD_1 | 113 | 115 | PF00675 | 0.717 |
CLV_NRD_NRD_1 | 197 | 199 | PF00675 | 0.611 |
CLV_NRD_NRD_1 | 259 | 261 | PF00675 | 0.516 |
CLV_NRD_NRD_1 | 449 | 451 | PF00675 | 0.628 |
CLV_PCSK_FUR_1 | 57 | 61 | PF00082 | 0.703 |
CLV_PCSK_KEX2_1 | 113 | 115 | PF00082 | 0.708 |
CLV_PCSK_KEX2_1 | 197 | 199 | PF00082 | 0.613 |
CLV_PCSK_KEX2_1 | 258 | 260 | PF00082 | 0.516 |
CLV_PCSK_KEX2_1 | 449 | 451 | PF00082 | 0.628 |
CLV_PCSK_KEX2_1 | 59 | 61 | PF00082 | 0.704 |
CLV_PCSK_PC1ET2_1 | 59 | 61 | PF00082 | 0.704 |
CLV_PCSK_PC7_1 | 254 | 260 | PF00082 | 0.449 |
CLV_PCSK_SKI1_1 | 364 | 368 | PF00082 | 0.631 |
CLV_PCSK_SKI1_1 | 59 | 63 | PF00082 | 0.627 |
DEG_SCF_FBW7_1 | 174 | 180 | PF00400 | 0.546 |
DEG_SCF_TRCP1_1 | 389 | 395 | PF00400 | 0.590 |
DEG_SPOP_SBC_1 | 122 | 126 | PF00917 | 0.580 |
DEG_SPOP_SBC_1 | 217 | 221 | PF00917 | 0.686 |
DEG_SPOP_SBC_1 | 92 | 96 | PF00917 | 0.666 |
DOC_CKS1_1 | 143 | 148 | PF01111 | 0.597 |
DOC_CKS1_1 | 174 | 179 | PF01111 | 0.550 |
DOC_CKS1_1 | 271 | 276 | PF01111 | 0.466 |
DOC_MAPK_DCC_7 | 258 | 267 | PF00069 | 0.585 |
DOC_MAPK_DCC_7 | 364 | 374 | PF00069 | 0.577 |
DOC_MAPK_gen_1 | 258 | 267 | PF00069 | 0.446 |
DOC_MAPK_MEF2A_6 | 258 | 267 | PF00069 | 0.585 |
DOC_MAPK_MEF2A_6 | 360 | 369 | PF00069 | 0.602 |
DOC_PP2B_PxIxI_1 | 262 | 268 | PF00149 | 0.576 |
DOC_USP7_MATH_1 | 152 | 156 | PF00917 | 0.575 |
DOC_USP7_MATH_1 | 229 | 233 | PF00917 | 0.583 |
DOC_USP7_MATH_1 | 298 | 302 | PF00917 | 0.568 |
DOC_USP7_MATH_1 | 43 | 47 | PF00917 | 0.569 |
DOC_USP7_MATH_1 | 92 | 96 | PF00917 | 0.667 |
DOC_WW_Pin1_4 | 123 | 128 | PF00397 | 0.715 |
DOC_WW_Pin1_4 | 134 | 139 | PF00397 | 0.592 |
DOC_WW_Pin1_4 | 142 | 147 | PF00397 | 0.620 |
DOC_WW_Pin1_4 | 170 | 175 | PF00397 | 0.626 |
DOC_WW_Pin1_4 | 231 | 236 | PF00397 | 0.560 |
DOC_WW_Pin1_4 | 270 | 275 | PF00397 | 0.566 |
DOC_WW_Pin1_4 | 392 | 397 | PF00397 | 0.588 |
LIG_14-3-3_CanoR_1 | 10 | 14 | PF00244 | 0.608 |
LIG_14-3-3_CanoR_1 | 187 | 196 | PF00244 | 0.646 |
LIG_14-3-3_CanoR_1 | 198 | 204 | PF00244 | 0.533 |
LIG_14-3-3_CanoR_1 | 207 | 217 | PF00244 | 0.506 |
LIG_14-3-3_CanoR_1 | 28 | 34 | PF00244 | 0.501 |
LIG_14-3-3_CanoR_1 | 353 | 362 | PF00244 | 0.610 |
LIG_14-3-3_CanoR_1 | 459 | 467 | PF00244 | 0.467 |
LIG_14-3-3_CanoR_1 | 97 | 101 | PF00244 | 0.656 |
LIG_Actin_RPEL_3 | 319 | 338 | PF02755 | 0.473 |
LIG_Actin_WH2_2 | 428 | 445 | PF00022 | 0.601 |
LIG_APCC_ABBA_1 | 428 | 433 | PF00400 | 0.610 |
LIG_FHA_1 | 143 | 149 | PF00498 | 0.717 |
LIG_FHA_2 | 43 | 49 | PF00498 | 0.559 |
LIG_FHA_2 | 468 | 474 | PF00498 | 0.593 |
LIG_LIR_Apic_2 | 12 | 16 | PF02991 | 0.608 |
LIG_LIR_Apic_2 | 269 | 274 | PF02991 | 0.608 |
LIG_LIR_Apic_2 | 481 | 487 | PF02991 | 0.617 |
LIG_LIR_Nem_3 | 249 | 253 | PF02991 | 0.499 |
LIG_Pex14_1 | 13 | 17 | PF04695 | 0.609 |
LIG_SH2_CRK | 271 | 275 | PF00017 | 0.606 |
LIG_SH2_GRB2like | 36 | 39 | PF00017 | 0.537 |
LIG_SH2_STAP1 | 409 | 413 | PF00017 | 0.444 |
LIG_SH2_STAT3 | 253 | 256 | PF00017 | 0.451 |
LIG_SH2_STAT5 | 65 | 68 | PF00017 | 0.615 |
LIG_SH3_3 | 138 | 144 | PF00018 | 0.702 |
LIG_SH3_3 | 171 | 177 | PF00018 | 0.611 |
LIG_SH3_3 | 182 | 188 | PF00018 | 0.654 |
LIG_SH3_3 | 219 | 225 | PF00018 | 0.625 |
LIG_SH3_3 | 390 | 396 | PF00018 | 0.592 |
LIG_SH3_3 | 424 | 430 | PF00018 | 0.570 |
LIG_SH3_3 | 66 | 72 | PF00018 | 0.615 |
LIG_SH3_3 | 98 | 104 | PF00018 | 0.701 |
LIG_SUMO_SIM_anti_2 | 422 | 428 | PF11976 | 0.451 |
LIG_TRAF2_1 | 155 | 158 | PF00917 | 0.571 |
LIG_TRAF2_1 | 346 | 349 | PF00917 | 0.610 |
LIG_TRAF2_1 | 470 | 473 | PF00917 | 0.595 |
LIG_TRFH_1 | 244 | 248 | PF08558 | 0.661 |
MOD_CK1_1 | 173 | 179 | PF00069 | 0.610 |
MOD_CK1_1 | 202 | 208 | PF00069 | 0.638 |
MOD_CK1_1 | 29 | 35 | PF00069 | 0.583 |
MOD_CK1_1 | 96 | 102 | PF00069 | 0.607 |
MOD_CK2_1 | 152 | 158 | PF00069 | 0.574 |
MOD_CK2_1 | 343 | 349 | PF00069 | 0.638 |
MOD_CK2_1 | 467 | 473 | PF00069 | 0.610 |
MOD_CK2_1 | 48 | 54 | PF00069 | 0.573 |
MOD_Cter_Amidation | 111 | 114 | PF01082 | 0.676 |
MOD_Cter_Amidation | 57 | 60 | PF01082 | 0.562 |
MOD_DYRK1A_RPxSP_1 | 142 | 146 | PF00069 | 0.576 |
MOD_GlcNHglycan | 130 | 134 | PF01048 | 0.812 |
MOD_GlcNHglycan | 150 | 153 | PF01048 | 0.665 |
MOD_GlcNHglycan | 154 | 157 | PF01048 | 0.693 |
MOD_GlcNHglycan | 160 | 164 | PF01048 | 0.646 |
MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.541 |
MOD_GlcNHglycan | 28 | 31 | PF01048 | 0.618 |
MOD_GlcNHglycan | 304 | 307 | PF01048 | 0.607 |
MOD_GlcNHglycan | 389 | 392 | PF01048 | 0.587 |
MOD_GlcNHglycan | 400 | 403 | PF01048 | 0.446 |
MOD_GlcNHglycan | 45 | 48 | PF01048 | 0.597 |
MOD_GlcNHglycan | 80 | 83 | PF01048 | 0.601 |
MOD_GlcNHglycan | 98 | 101 | PF01048 | 0.700 |
MOD_GSK3_1 | 148 | 155 | PF00069 | 0.617 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.625 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.619 |
MOD_GSK3_1 | 198 | 205 | PF00069 | 0.556 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.641 |
MOD_GSK3_1 | 242 | 249 | PF00069 | 0.656 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.582 |
MOD_GSK3_1 | 324 | 331 | PF00069 | 0.624 |
MOD_GSK3_1 | 383 | 390 | PF00069 | 0.556 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.694 |
MOD_N-GLC_1 | 217 | 222 | PF02516 | 0.554 |
MOD_NEK2_1 | 148 | 153 | PF00069 | 0.603 |
MOD_NEK2_2 | 242 | 247 | PF00069 | 0.644 |
MOD_PIKK_1 | 116 | 122 | PF00454 | 0.599 |
MOD_PKA_2 | 246 | 252 | PF00069 | 0.615 |
MOD_PKA_2 | 458 | 464 | PF00069 | 0.461 |
MOD_PKA_2 | 9 | 15 | PF00069 | 0.609 |
MOD_PKA_2 | 96 | 102 | PF00069 | 0.656 |
MOD_Plk_1 | 129 | 135 | PF00069 | 0.579 |
MOD_Plk_1 | 217 | 223 | PF00069 | 0.556 |
MOD_Plk_2-3 | 324 | 330 | PF00069 | 0.626 |
MOD_Plk_4 | 383 | 389 | PF00069 | 0.518 |
MOD_ProDKin_1 | 123 | 129 | PF00069 | 0.715 |
MOD_ProDKin_1 | 134 | 140 | PF00069 | 0.593 |
MOD_ProDKin_1 | 142 | 148 | PF00069 | 0.620 |
MOD_ProDKin_1 | 170 | 176 | PF00069 | 0.627 |
MOD_ProDKin_1 | 231 | 237 | PF00069 | 0.560 |
MOD_ProDKin_1 | 270 | 276 | PF00069 | 0.567 |
MOD_ProDKin_1 | 392 | 398 | PF00069 | 0.580 |
TRG_ENDOCYTIC_2 | 335 | 338 | PF00928 | 0.625 |
TRG_ER_diArg_1 | 113 | 115 | PF00400 | 0.678 |
TRG_ER_diArg_1 | 196 | 198 | PF00400 | 0.640 |
TRG_ER_diArg_1 | 257 | 260 | PF00400 | 0.526 |
TRG_ER_diArg_1 | 449 | 451 | PF00400 | 0.628 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S5H5D8 | Leishmania donovani | 66% | 97% |
A4HS94 | Leishmania infantum | 65% | 100% |
E9AK78 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 66% | 100% |
Q9U1D2 | Leishmania major | 68% | 98% |