GapMind for catabolism of small carbon sources

 

Alignments for a candidate for malK in Alicycliphilus denitrificans K601

Align Maltose-transporting ATPase (EC 3.6.3.19) (characterized)
to candidate WP_013517832.1 ALIDE2_RS04530 sn-glycerol-3-phosphate ABC transporter ATP-binding protein UgpC

Query= reanno::psRCH2:GFF857
         (371 letters)



>NCBI__GCF_000204645.1:WP_013517832.1
          Length = 335

 Score =  313 bits (802), Expect = 4e-90
 Identities = 174/357 (48%), Positives = 228/357 (63%), Gaps = 34/357 (9%)

Query: 1   MASVTLRDICKSY----DGTPITRHIDLDIEDGEFVVFVGPSGCGKSTLLRLIAGLEDIT 56
           MAS++L++I K Y       P+   ++ +I+DGEF+V VGPSGCGKSTLLR+IAGLE+IT
Sbjct: 1   MASISLKNIVKRYGSGKSAVPVIHGVNAEIKDGEFIVLVGPSGCGKSTLLRMIAGLEEIT 60

Query: 57  SGDLLIDNQRVNDLPPKDRSVGMVFQSYALYPHMTVAENMAFGLKLASVDKREIKRRVEA 116
            G+L I ++ VN L P  R++ MVFQ+YALYPHMT  ENMA+GLKLA V K EI+RRV+ 
Sbjct: 61  GGELFIGDRLVNGLEPARRNIAMVFQNYALYPHMTNFENMAYGLKLAKVPKDEIRRRVDK 120

Query: 117 VAEILQLDKLLERKPKDLSGGQRQRVAIGRTMVREPKVFLFDEPLSNLDAFLRVQMRIEI 176
            A+IL+L  LLERKP++LSGGQRQRVA+GR +VREP+VFLFDEPLSNLDA LR Q RIEI
Sbjct: 121 AAKILELSHLLERKPRELSGGQRQRVAMGRAIVREPQVFLFDEPLSNLDAKLRGQTRIEI 180

Query: 177 ARLHQRIRSTMIYVTHDQVEAMTLADKIVVLNAGEIAQVGQPLHLYHYPKNRFVAGFLGS 236
            +LH  +  T ++VTHDQVEAMTLA +++V+NAG + Q G P  +YH P   FVA F+GS
Sbjct: 181 QKLHTELGITSLFVTHDQVEAMTLAQRMIVMNAGNVEQFGTPEEVYHEPATTFVASFIGS 240

Query: 237 PQMNFVEVRAISASPETVTIELPSGYPLTLPVDGSAVSPGDPLTLGIRPEHFVMPDEADF 296
           P MN ++             + P G P  +              LGIRPEH  + +   +
Sbjct: 241 PPMNLLK-------------QAPGGQPGRI--------------LGIRPEHIDLVESGGW 273

Query: 297 TFHGQITVAERLGQYNLLYLTLERLQDVITLCVDGNLRVTEGETFAAGLKADKCHLF 353
            F  ++   E LG   LLY  +   +D+     +       GET     + D+ H F
Sbjct: 274 EF--KVETLELLGAERLLYGKVGD-EDLTVRTEEDKPYPKPGETTRIAPRRDRVHWF 327


Lambda     K      H
   0.322    0.139    0.405 

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: 369
Number of extensions: 13
Number of successful extensions: 2
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: 371
Length of database: 335
Length adjustment: 29
Effective length of query: 342
Effective length of database: 306
Effective search space:   104652
Effective search space used:   104652
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.9 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Apr 09 2024. 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