Align NatB aka SLR0559, component of Leucine/proline/alanine/serine/glycine (and possibly histidine) porter, NatABCDE (characterized)
to candidate Synpcc7942_1861 Synpcc7942_1861 periplasmic binding protein of ABC transporter for natural amino acids
Query= TCDB::Q55387 (454 letters) >lcl|FitnessBrowser__SynE:Synpcc7942_1861 Synpcc7942_1861 periplasmic binding protein of ABC transporter for natural amino acids Length = 421 Score = 354 bits (909), Expect = e-102 Identities = 179/384 (46%), Positives = 254/384 (66%), Gaps = 2/384 (0%) Query: 63 GALKLGALLPATGDLSSIGQNMPLAVQLAVDTINACGGVNGQDVTVVIEDDQTDPTAGVS 122 G LKLG+LLP TGDL+ G+ M +L V T+NACGGV G V ++ DD+T P GV+ Sbjct: 33 GGLKLGSLLPLTGDLAQYGRPMQDTAELLVQTVNACGGVQGLPVRLIPADDETKPDRGVA 92 Query: 123 AMTKLAEADQVAGVVGSFASSVSSAAVPIAVRNNIMMISPGSTSPVFTDQAKKGEFKGFW 182 AMTKLAE D+VAGVVG+ AS+VS AA+ +AV N ++MISP STSP FT++A++G+FKG+W Sbjct: 93 AMTKLAEVDRVAGVVGAAASNVSDAALTLAVNNRVVMISPSSTSPRFTERARRGDFKGYW 152 Query: 183 ARTAPPDTYQAQALAALAKKQGFTDAATVVINNDYGVGFEKVFVESFTADGGNVTNKDNP 242 RTAP D Q ALA LA QG+ + + INNDYG G + F+ +F GG V N+D P Sbjct: 153 FRTAPSDALQGPALAKLALDQGWRSVSVIAINNDYGNGLLRSFIPAFEQAGGVVFNRDQP 212 Query: 243 VRYDPKAATLDTEAAQGFANSPDAVAAILYADTGSVLVQSAYRQGLMDGVT-LLLTDGVY 301 V Y P A++ D+E Q F + PDAV I Y D+G+++++SAY +GL+ T +LLTDG+ Sbjct: 213 VLYTPDASSFDSEVEQVFRDRPDAVVLIGYPDSGALILKSAYEKGLLGQSTQMLLTDGLK 272 Query: 302 SPDFVEKVGKDANGVSLLSGALGTVPGADGKSLEAFTAQWKDATGGKDVTAFVPHTYDAT 361 + E VG++ G ++ +G P + G EAF ++++ + F +T+DA Sbjct: 273 TDQLAELVGRNPQGRYIVQDLVGVAPSSGGPGREAFLKRYQERF-QRSPQVFDANTWDAA 331 Query: 362 VLMMLAAEAAKSNTGAGIQSKIRDVSNGPGEEVTDACEAIAMVREGKDINYQGASGNVDI 421 L++LAAE +KS G ++ + ++NGPGE V+D C+A+A+VR GK INYQGAS + + Sbjct: 332 ALLVLAAEKSKSLEGEKLKDSVAAIANGPGEPVSDICQALALVRAGKPINYQGASSELKL 391 Query: 422 DENGDVVGTYDVWTVKGDGTLEVI 445 D NGDV G YD W DG ++++ Sbjct: 392 DNNGDVSGRYDFWQFDADGKVKIL 415 Lambda K H 0.313 0.131 0.374 Gapped Lambda K H 0.267 0.0410 0.140 Matrix: BLOSUM62 Gap Penalties: Existence: 11, Extension: 1 Number of Sequences: 1 Number of Hits to DB: 456 Number of extensions: 20 Number of successful extensions: 3 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 1 Number of HSP's successfully gapped: 1 Length of query: 454 Length of database: 421 Length adjustment: 32 Effective length of query: 422 Effective length of database: 389 Effective search space: 164158 Effective search space used: 164158 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.2 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 42 (21.9 bits) S2: 51 (24.3 bits)
This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.
Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.
A candidate for a step is "high confidence" if either:
Otherwise, a candidate is "medium confidence" if either:
Other blast hits with at least 50% coverage are "low confidence."
Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:
GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).
For more information, see the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.
If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know
by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory