Uncharacterized Protein, Uncharacterized
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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0030990 | intraciliary transport particle | 2 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
Related structures:
AlphaFold database: A4I7K0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 319 | 323 | PF00656 | 0.787 |
CLV_NRD_NRD_1 | 18 | 20 | PF00675 | 0.447 |
CLV_NRD_NRD_1 | 236 | 238 | PF00675 | 0.613 |
CLV_NRD_NRD_1 | 249 | 251 | PF00675 | 0.546 |
CLV_PCSK_FUR_1 | 149 | 153 | PF00082 | 0.699 |
CLV_PCSK_KEX2_1 | 151 | 153 | PF00082 | 0.633 |
CLV_PCSK_KEX2_1 | 18 | 20 | PF00082 | 0.428 |
CLV_PCSK_KEX2_1 | 249 | 251 | PF00082 | 0.646 |
CLV_PCSK_KEX2_1 | 340 | 342 | PF00082 | 0.793 |
CLV_PCSK_PC1ET2_1 | 151 | 153 | PF00082 | 0.672 |
CLV_PCSK_PC1ET2_1 | 340 | 342 | PF00082 | 0.793 |
CLV_PCSK_SKI1_1 | 152 | 156 | PF00082 | 0.694 |
CLV_PCSK_SKI1_1 | 237 | 241 | PF00082 | 0.614 |
CLV_PCSK_SKI1_1 | 249 | 253 | PF00082 | 0.595 |
DEG_APCC_DBOX_1 | 248 | 256 | PF00400 | 0.628 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.643 |
DOC_ANK_TNKS_1 | 94 | 101 | PF00023 | 0.719 |
DOC_CYCLIN_RxL_1 | 128 | 136 | PF00134 | 0.502 |
DOC_USP7_MATH_1 | 284 | 288 | PF00917 | 0.677 |
DOC_USP7_MATH_1 | 313 | 317 | PF00917 | 0.713 |
DOC_USP7_MATH_1 | 99 | 103 | PF00917 | 0.743 |
DOC_WW_Pin1_4 | 343 | 348 | PF00397 | 0.669 |
DOC_WW_Pin1_4 | 54 | 59 | PF00397 | 0.503 |
LIG_14-3-3_CanoR_1 | 140 | 146 | PF00244 | 0.502 |
LIG_14-3-3_CanoR_1 | 152 | 162 | PF00244 | 0.614 |
LIG_14-3-3_CanoR_1 | 18 | 22 | PF00244 | 0.457 |
LIG_14-3-3_CanoR_1 | 237 | 244 | PF00244 | 0.636 |
LIG_14-3-3_CanoR_1 | 293 | 297 | PF00244 | 0.686 |
LIG_14-3-3_CanoR_1 | 90 | 99 | PF00244 | 0.734 |
LIG_Clathr_ClatBox_1 | 132 | 136 | PF01394 | 0.480 |
LIG_CSL_BTD_1 | 305 | 308 | PF09270 | 0.721 |
LIG_FHA_2 | 202 | 208 | PF00498 | 0.555 |
LIG_FHA_2 | 230 | 236 | PF00498 | 0.538 |
LIG_LIR_Apic_2 | 294 | 299 | PF02991 | 0.687 |
LIG_LIR_Apic_2 | 60 | 66 | PF02991 | 0.665 |
LIG_NRBOX | 128 | 134 | PF00104 | 0.457 |
LIG_NRBOX | 251 | 257 | PF00104 | 0.627 |
LIG_PTAP_UEV_1 | 307 | 312 | PF05743 | 0.651 |
LIG_SH2_SRC | 296 | 299 | PF00017 | 0.732 |
LIG_SH2_STAT3 | 5 | 8 | PF00017 | 0.674 |
LIG_SH2_STAT5 | 169 | 172 | PF00017 | 0.725 |
LIG_SH2_STAT5 | 87 | 90 | PF00017 | 0.625 |
LIG_SH3_3 | 213 | 219 | PF00018 | 0.622 |
LIG_SH3_3 | 302 | 308 | PF00018 | 0.683 |
LIG_SH3_3 | 55 | 61 | PF00018 | 0.635 |
LIG_SUMO_SIM_anti_2 | 322 | 329 | PF11976 | 0.668 |
LIG_SUMO_SIM_par_1 | 130 | 136 | PF11976 | 0.480 |
LIG_SUMO_SIM_par_1 | 322 | 329 | PF11976 | 0.566 |
LIG_UBA3_1 | 132 | 138 | PF00899 | 0.507 |
MOD_CK1_1 | 156 | 162 | PF00069 | 0.669 |
MOD_CK1_1 | 17 | 23 | PF00069 | 0.478 |
MOD_CK1_1 | 171 | 177 | PF00069 | 0.745 |
MOD_CK1_1 | 316 | 322 | PF00069 | 0.767 |
MOD_CK2_1 | 107 | 113 | PF00069 | 0.622 |
MOD_CK2_1 | 180 | 186 | PF00069 | 0.785 |
MOD_CK2_1 | 201 | 207 | PF00069 | 0.561 |
MOD_CK2_1 | 275 | 281 | PF00069 | 0.747 |
MOD_GlcNHglycan | 155 | 158 | PF01048 | 0.657 |
MOD_GlcNHglycan | 170 | 173 | PF01048 | 0.678 |
MOD_GlcNHglycan | 179 | 183 | PF01048 | 0.732 |
MOD_GlcNHglycan | 277 | 280 | PF01048 | 0.737 |
MOD_GlcNHglycan | 311 | 314 | PF01048 | 0.670 |
MOD_GlcNHglycan | 329 | 333 | PF01048 | 0.720 |
MOD_GlcNHglycan | 337 | 340 | PF01048 | 0.674 |
MOD_GlcNHglycan | 35 | 38 | PF01048 | 0.651 |
MOD_GlcNHglycan | 50 | 53 | PF01048 | 0.575 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.703 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.680 |
MOD_GSK3_1 | 167 | 174 | PF00069 | 0.648 |
MOD_GSK3_1 | 309 | 316 | PF00069 | 0.709 |
MOD_N-GLC_1 | 107 | 112 | PF02516 | 0.602 |
MOD_N-GLC_1 | 152 | 157 | PF02516 | 0.732 |
MOD_N-GLC_1 | 67 | 72 | PF02516 | 0.540 |
MOD_N-GLC_1 | 90 | 95 | PF02516 | 0.704 |
MOD_N-GLC_2 | 42 | 44 | PF02516 | 0.592 |
MOD_N-GLC_2 | 45 | 47 | PF02516 | 0.605 |
MOD_NEK2_1 | 14 | 19 | PF00069 | 0.377 |
MOD_NEK2_1 | 178 | 183 | PF00069 | 0.756 |
MOD_NEK2_1 | 26 | 31 | PF00069 | 0.478 |
MOD_NEK2_1 | 285 | 290 | PF00069 | 0.666 |
MOD_NEK2_1 | 33 | 38 | PF00069 | 0.438 |
MOD_NEK2_1 | 72 | 77 | PF00069 | 0.557 |
MOD_NEK2_2 | 107 | 112 | PF00069 | 0.777 |
MOD_PIKK_1 | 138 | 144 | PF00454 | 0.589 |
MOD_PIKK_1 | 26 | 32 | PF00454 | 0.552 |
MOD_PIKK_1 | 313 | 319 | PF00454 | 0.761 |
MOD_PIKK_1 | 99 | 105 | PF00454 | 0.712 |
MOD_PKA_1 | 237 | 243 | PF00069 | 0.624 |
MOD_PKA_2 | 17 | 23 | PF00069 | 0.462 |
MOD_PKA_2 | 292 | 298 | PF00069 | 0.672 |
MOD_Plk_1 | 67 | 73 | PF00069 | 0.629 |
MOD_Plk_2-3 | 201 | 207 | PF00069 | 0.488 |
MOD_ProDKin_1 | 343 | 349 | PF00069 | 0.671 |
MOD_ProDKin_1 | 54 | 60 | PF00069 | 0.499 |
MOD_SUMO_rev_2 | 130 | 139 | PF00179 | 0.481 |
TRG_DiLeu_BaLyEn_6 | 128 | 133 | PF01217 | 0.478 |
TRG_NES_CRM1_1 | 125 | 136 | PF08389 | 0.483 |
TRG_Pf-PMV_PEXEL_1 | 131 | 136 | PF00026 | 0.479 |
TRG_Pf-PMV_PEXEL_1 | 250 | 254 | PF00026 | 0.602 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8J4 | Leptomonas seymouri | 59% | 98% |
A0A1X0P6Q1 | Trypanosomatidae | 37% | 86% |
A0A3Q8IGR0 | Leishmania donovani | 99% | 100% |
A0A3R7RRK4 | Trypanosoma rangeli | 36% | 92% |
A4HK16 | Leishmania braziliensis | 78% | 98% |
D0A0A3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
E9B2F7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q4Q5P9 | Leishmania major | 95% | 100% |