GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xylF in Rhodobacter johrii JA192

Align D-xylose ABC transporter, periplasmic substrate-binding protein, component of Xylose transporter, XylFGH (XylF (R), 359 aas; XylG (C), 525 aas; XylH (M), 389 aas (characterized)
to candidate WP_069330983.1 C8J29_RS17285 sugar ABC transporter substrate-binding protein

Query= TCDB::A6LW10
         (359 letters)



>NCBI__GCF_003046325.1:WP_069330983.1
          Length = 349

 Score =  163 bits (413), Expect = 6e-45
 Identities = 105/299 (35%), Positives = 158/299 (52%), Gaps = 17/299 (5%)

Query: 57  QHDKEIFEEEAKKLGAD--VVFQSANGDDPTQMSQAENLISQGVDVLVVIPHNGESIAPI 114
           +HD   F++   +L  D  V++Q+ANGD   Q  Q  ++I+QG  ++V+ P +  + A +
Sbjct: 45  EHDFPGFQKSMGELCPDCTVIYQNANGDVALQQQQFNSVIAQGAKIVVLDPVDSAAAASM 104

Query: 115 VEEAHQNKIKVLAYDRLITNSDLDYYVSFDNVKVGELQAKAIVDK-----TPKG-NYFMM 168
           VE AH   +KV+AYDR I  +  DYYVSFDN  +G+  A+++VD       P G     +
Sbjct: 105 VEIAHSQDVKVIAYDRPIPATPADYYVSFDNKGIGQAIAQSLVDHLKATGVPDGAGVLQI 164

Query: 169 GGSPTDNNAKLFRQGQMNIIKPYVDKGDIKLVGDQWVKDWSAEEALKIMENALTANNNKL 228
            GSPTD  A L R G    I   +D    K + +    DW+  +A +     +T   +++
Sbjct: 165 NGSPTDAAAGLIRDG----IDAALDASGYKTLAEFDTPDWAPPKAQEWAAGQITRFGDEI 220

Query: 229 DAVVASNDSTAGGAIQALQAQSLAGKITISGQDADLAGCQRVVEGTQTMTIYKPIKDIAA 288
             VVA+ND T GGAI A +A  +     ++G DA +A  Q ++ G Q  TI KP + +A 
Sbjct: 221 KGVVAANDGTGGGAIAAFKAAGVDPVPPVTGNDATIAALQLIISGDQYNTISKPSEIVAE 280

Query: 289 KAAEMAVKMAKGEDVETGGTVTNNGKKDVPSVLLTPIAVTADNMKDTVIKDGFQKFDDV 347
            AA++AV   KGE  E   T+      D P+ L  P  VTA+N+K  +   G Q   +V
Sbjct: 281 AAAKVAVTFLKGETPEAKTTL-----YDTPAELFVPAVVTAENIKAEIFDKGIQTAAEV 334


Lambda     K      H
   0.312    0.130    0.360 

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: 290
Number of extensions: 12
Number of successful extensions: 4
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: 359
Length of database: 349
Length adjustment: 29
Effective length of query: 330
Effective length of database: 320
Effective search space:   105600
Effective search space used:   105600
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: 49 (23.5 bits)

This GapMind analysis is from Sep 24 2021. The underlying query database was built on Sep 17 2021.

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About GapMind

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:

where "other" refers to the best ublast hit to a sequence that is not annotated as performing this step (and is not "ignored").

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:

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