GapMind for catabolism of small carbon sources

 

Alignments for a candidate for malK in Phyllobacterium brassicacearum STM 196

Align Maltose/maltodextrin import ATP-binding protein MalK; EC 7.5.2.1 (characterized)
to candidate WP_106713056.1 CU102_RS21035 ABC transporter ATP-binding protein

Query= SwissProt::P19566
         (369 letters)



>NCBI__GCF_003010955.1:WP_106713056.1
          Length = 355

 Score =  335 bits (858), Expect = 1e-96
 Identities = 184/358 (51%), Positives = 242/358 (67%), Gaps = 8/358 (2%)

Query: 1   MASVQLRNVTKAWGDVVVSKDINLDIHDGEFVVFVGPSGCGKSTLLRMIAGLETITSGDL 60
           M  ++L NV K++G V V  DI+L+I D EFVVFVGPSGCGKSTLLRMIAGL+  + G+L
Sbjct: 1   MGHIKLTNVAKSFGSVDVLHDISLEIADSEFVVFVGPSGCGKSTLLRMIAGLDRPSRGEL 60

Query: 61  FIGETRMNDIPPAERGVGMVFQSYALYPHLSVAENMSFGLKLAGAKKEVMNQRVNQVAEV 120
            I    +N++P A+RG+ MVFQSYALYPH+SV +N++FGL+     K  + +R+ + A +
Sbjct: 61  TIDGKLVNNVPAADRGLAMVFQSYALYPHMSVRQNLAFGLENTKMPKAEIVERIAEAARM 120

Query: 121 LQLAHLLERKPKALSGGQRQRVAIGRTLVAEPRVFLLDEPLSNLDAALRVQMRIEISRLH 180
           L++   LER+P  LSGGQRQRVAIGR +V  P  FLLDEPLSNLDA LR   R E++ LH
Sbjct: 121 LEIEPYLERRPGQLSGGQRQRVAIGRAIVRRPVAFLLDEPLSNLDAELRGSTRAELAALH 180

Query: 181 KRLGRTMIYVTHDQVEAMTLADKIVVLDAGRVAQVGKPLELYHYPADRFVAGFIGSPKMN 240
            RL  TMIYVTHDQVEAMTLAD+IVVL AGRV QVG PLELY+ PA+RFVAGFIGSP MN
Sbjct: 181 ARLSATMIYVTHDQVEAMTLADRIVVLRAGRVEQVGTPLELYNSPANRFVAGFIGSPHMN 240

Query: 241 FLPVKVTATAIEQVQVELPNRQQIWLPVESRGVQVGANMSLGIRPEHLLPSDIADVTLEG 300
           FL   + +    +  V L    ++ +PV+  G   GA ++LG+RP+H+   D   +    
Sbjct: 241 FLDGTIESLGPSKAVVALTGGHRVEVPVD--GTAAGARVTLGVRPQHISIGDKQGI--PA 296

Query: 301 EVQVVEQLGHETQIHIQIPAIRQNLVY-RQNDVVLVEEGATFAIGLPPERCHLFREDG 357
           E+++VE LG ET +H  +   +  +V   Q+D++    GA   + L     H+F E G
Sbjct: 297 EIKLVEALGSETVLHADVAGQKVLVVAPGQHDLM---AGAGIHLSLSAAPLHIFNEQG 351


Lambda     K      H
   0.321    0.138    0.396 

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: 379
Number of extensions: 16
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: 369
Length of database: 355
Length adjustment: 29
Effective length of query: 340
Effective length of database: 326
Effective search space:   110840
Effective search space used:   110840
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 (21.8 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