GapMind for catabolism of small carbon sources

 

Alignments for a candidate for PGA1_c07310 in Herbaspirillum seropedicae SmR1

Align Inositol transport system permease protein (characterized)
to candidate HSERO_RS12115 HSERO_RS12115 ATPase

Query= reanno::Phaeo:GFF716
         (373 letters)



>FitnessBrowser__HerbieS:HSERO_RS12115
          Length = 379

 Score =  400 bits (1027), Expect = e-116
 Identities = 202/361 (55%), Positives = 254/361 (70%), Gaps = 5/361 (1%)

Query: 11  DERIKTRSKFREAMIRPELGGIIGTITVFAMFLIFAGDSGMFNSQGVMNWSQISAQFMII 70
           DER++  +     + RPE   + G I VF +F + AGDSGMFN  GV+NW Q++A   II
Sbjct: 20  DERMRRENLVSRLLGRPEFASLAGVILVFLVFGLTAGDSGMFNLDGVVNWMQVAAYLGII 79

Query: 71  AVGACLLMIAGEFDLSVGSMIGFAGMLIAIFSVTLGWPVWLAILVTFAIATAIGALNGFI 130
           AV ACLLMI GEFDLS+GSMIG AGM++AI +V  GWP WLA+L  FA +  +G LNG++
Sbjct: 80  AVAACLLMIGGEFDLSIGSMIGLAGMMVAIPTVYFGWPFWLAVLFAFAASMGLGWLNGYL 139

Query: 131 VVRTGLPSFIVTLAFLFILRGFAIYLPQTIERKTIIGGVADAAEGDWLAAL-FGGKILTG 189
           V++T LPSFIVTLAFLFILRG  + L      +TI+ GV + A  DWL  L F G +  G
Sbjct: 140 VMKTRLPSFIVTLAFLFILRGLTLALSILFANRTIVSGVGERAAHDWLGQLLFSGNVGAG 199

Query: 190 LFQWFGDNGWIAVFERGTRKGQPVVEGLPMLIVWAILLVIIGHVILTKTRFGNWIFAAGG 249
           LF W   +GWIA    GT    P+V G+P +I+W  ++ +    +L +TR GNWIFA GG
Sbjct: 200 LFSWLARHGWIATVADGT----PLVTGIPKVILWWAVVALAASFVLARTRLGNWIFAVGG 255

Query: 250 DAEAARNSGVPVNRVKILMFMFTAFCATVFATCQVMEFGGAGSDRGLLKEFEAIIAVVIG 309
           DA AA+N GVPV +VKI +F+FTAFCA +FA  QV +FG A +DRGL KEFEAIIA VIG
Sbjct: 256 DAVAAKNMGVPVRKVKIGLFVFTAFCACLFAVLQVGDFGSAAADRGLQKEFEAIIAAVIG 315

Query: 310 GALLTGGYGSVLGAALGALIFGVVQQGLFFAGVESSLFRVFLGLILLFAVILNTYIRRVI 369
           GALLTGGYGSV+GA  GALIFGVVQ G+ +  + S  FRVFLG++LL AV+ N ++RR I
Sbjct: 316 GALLTGGYGSVIGACFGALIFGVVQIGITYTNLSSDWFRVFLGVMLLVAVLFNNFVRRRI 375

Query: 370 T 370
           T
Sbjct: 376 T 376


Lambda     K      H
   0.330    0.145    0.443 

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: 599
Number of extensions: 37
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: 373
Length of database: 379
Length adjustment: 30
Effective length of query: 343
Effective length of database: 349
Effective search space:   119707
Effective search space used:   119707
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.1 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.8 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Sep 17 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